Genomic Sequencing to Detect Cross-Breeding Quality in Dogs: An Example Studying Disorders in Sexual Development
Disorders of sexual development (DSDs) in dogs, similar to humans, arise from genetic mutations, gonadal differentiation, or phenotypic sex development. The French Bulldog, a breed that has seen a surge in popularity and demand, has also shown a marked increase in DSD incidence. This study aims to c...
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creator | de Gennaro, Luciana Burgio, Matteo Lacalandra, Giovanni Michele Petronella, Francesco L'Abbate, Alberto Ravasini, Francesco Trombetta, Beniamino Rizzo, Annalisa Ventura, Mario Cicirelli, Vincenzo |
description | Disorders of sexual development (DSDs) in dogs, similar to humans, arise from genetic mutations, gonadal differentiation, or phenotypic sex development. The French Bulldog, a breed that has seen a surge in popularity and demand, has also shown a marked increase in DSD incidence. This study aims to characterize the genetic underpinnings of DSDs in a French Bulldog named
, exhibiting ambiguous genitalia and internal sexual anatomy, and to explore the impact of breeding practices on genetic diversity within the breed. We utilized a comprehensive approach combining conventional cytogenetics, molecular techniques, and deep sequencing to investigate the genetic profile of
. The sequence data were compared to three other male French Bulldogs' genome sequences with typical reproductive anatomy, including
's father and the canine reference genome (CanFam6). We found a Robertsonian fusion involving chromosome 23 previously reported in dogs as a causative mutation responsible for sex reversal syndrome. Our findings revealed a 22% mosaicism (78,XX/77,XX), the absence of the sex-determining region (
) gene, and the presence of 43 unique Single Nucleotide Variants (SNVs) not inherited from the father. Notably, the run of homozygosity (ROH) analysis showed
has a higher number of homozygous segments compared to other Bulldogs, with a total length of these fragments 50% greater than the average, strongly suggesting this dog is the product of the mating between siblings. Although no direct causative genes for the DSD phenotype were identified, four candidate loci warrant further investigation. Our study highlighted the need for a better annotated and curated reference dog genome to define genes causative of any specific phenotype, suggests a potential genetic basis for the DSD phenotype in dogs, and underscores the consequences of uncontrolled breeding practices in French Bulldogs. These findings highlight the importance of implementing strategic genetic management to preserve genetic health and diversity in canine populations. |
doi_str_mv | 10.3390/ijms251910763 |
format | Article |
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, exhibiting ambiguous genitalia and internal sexual anatomy, and to explore the impact of breeding practices on genetic diversity within the breed. We utilized a comprehensive approach combining conventional cytogenetics, molecular techniques, and deep sequencing to investigate the genetic profile of
. The sequence data were compared to three other male French Bulldogs' genome sequences with typical reproductive anatomy, including
's father and the canine reference genome (CanFam6). We found a Robertsonian fusion involving chromosome 23 previously reported in dogs as a causative mutation responsible for sex reversal syndrome. Our findings revealed a 22% mosaicism (78,XX/77,XX), the absence of the sex-determining region (
) gene, and the presence of 43 unique Single Nucleotide Variants (SNVs) not inherited from the father. Notably, the run of homozygosity (ROH) analysis showed
has a higher number of homozygous segments compared to other Bulldogs, with a total length of these fragments 50% greater than the average, strongly suggesting this dog is the product of the mating between siblings. Although no direct causative genes for the DSD phenotype were identified, four candidate loci warrant further investigation. Our study highlighted the need for a better annotated and curated reference dog genome to define genes causative of any specific phenotype, suggests a potential genetic basis for the DSD phenotype in dogs, and underscores the consequences of uncontrolled breeding practices in French Bulldogs. These findings highlight the importance of implementing strategic genetic management to preserve genetic health and diversity in canine populations.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms251910763</identifier><identifier>PMID: 39409092</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Animals ; Breeding ; Causes of ; Disorders of Sex Development - genetics ; Disorders of Sex Development - veterinary ; DNA sequencing ; Dog breeding ; Dog Diseases - genetics ; Dogs ; Female ; Genes ; Genetic aspects ; Genome ; Genomes ; Genomics - methods ; High-Throughput Nucleotide Sequencing ; Male ; Methods ; Mitochondrial DNA ; Mutation ; Nucleotide sequencing ; Penis ; Phenotype ; Polymorphism, Single Nucleotide ; Pseudohermaphroditism ; Sex chromosomes ; Sex differentiation disorders ; X chromosomes</subject><ispartof>International journal of molecular sciences, 2024-10, Vol.25 (19), p.10763</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c369t-81b20e58f6cf2c9981cac604cddf3f5db9371d2e33abdc1a937ae198d6f395d03</cites><orcidid>0000-0003-2792-8848 ; 0000-0002-2688-0056 ; 0009-0007-9572-7630 ; 0000-0002-5995-2001 ; 0000-0001-7762-8777 ; 0000-0002-8203-4540 ; 0000-0001-9109-3561 ; 0000-0003-2866-5533</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11476854/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11476854/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39409092$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Gennaro, Luciana</creatorcontrib><creatorcontrib>Burgio, Matteo</creatorcontrib><creatorcontrib>Lacalandra, Giovanni Michele</creatorcontrib><creatorcontrib>Petronella, Francesco</creatorcontrib><creatorcontrib>L'Abbate, Alberto</creatorcontrib><creatorcontrib>Ravasini, Francesco</creatorcontrib><creatorcontrib>Trombetta, Beniamino</creatorcontrib><creatorcontrib>Rizzo, Annalisa</creatorcontrib><creatorcontrib>Ventura, Mario</creatorcontrib><creatorcontrib>Cicirelli, Vincenzo</creatorcontrib><title>Genomic Sequencing to Detect Cross-Breeding Quality in Dogs: An Example Studying Disorders in Sexual Development</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Disorders of sexual development (DSDs) in dogs, similar to humans, arise from genetic mutations, gonadal differentiation, or phenotypic sex development. The French Bulldog, a breed that has seen a surge in popularity and demand, has also shown a marked increase in DSD incidence. This study aims to characterize the genetic underpinnings of DSDs in a French Bulldog named
, exhibiting ambiguous genitalia and internal sexual anatomy, and to explore the impact of breeding practices on genetic diversity within the breed. We utilized a comprehensive approach combining conventional cytogenetics, molecular techniques, and deep sequencing to investigate the genetic profile of
. The sequence data were compared to three other male French Bulldogs' genome sequences with typical reproductive anatomy, including
's father and the canine reference genome (CanFam6). We found a Robertsonian fusion involving chromosome 23 previously reported in dogs as a causative mutation responsible for sex reversal syndrome. Our findings revealed a 22% mosaicism (78,XX/77,XX), the absence of the sex-determining region (
) gene, and the presence of 43 unique Single Nucleotide Variants (SNVs) not inherited from the father. Notably, the run of homozygosity (ROH) analysis showed
has a higher number of homozygous segments compared to other Bulldogs, with a total length of these fragments 50% greater than the average, strongly suggesting this dog is the product of the mating between siblings. Although no direct causative genes for the DSD phenotype were identified, four candidate loci warrant further investigation. Our study highlighted the need for a better annotated and curated reference dog genome to define genes causative of any specific phenotype, suggests a potential genetic basis for the DSD phenotype in dogs, and underscores the consequences of uncontrolled breeding practices in French Bulldogs. These findings highlight the importance of implementing strategic genetic management to preserve genetic health and diversity in canine populations.</description><subject>Animals</subject><subject>Breeding</subject><subject>Causes of</subject><subject>Disorders of Sex Development - genetics</subject><subject>Disorders of Sex Development - veterinary</subject><subject>DNA sequencing</subject><subject>Dog breeding</subject><subject>Dog Diseases - genetics</subject><subject>Dogs</subject><subject>Female</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genome</subject><subject>Genomes</subject><subject>Genomics - methods</subject><subject>High-Throughput Nucleotide Sequencing</subject><subject>Male</subject><subject>Methods</subject><subject>Mitochondrial DNA</subject><subject>Mutation</subject><subject>Nucleotide sequencing</subject><subject>Penis</subject><subject>Phenotype</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Pseudohermaphroditism</subject><subject>Sex chromosomes</subject><subject>Sex differentiation disorders</subject><subject>X chromosomes</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkk1v1DAQhi1ERUvhyBVZ4sIlxR-JE3NB291SKlVCaNuz5bUni1eJHeyk6v57HLWULkI-2ON55h3NB0LvKDnjXJJPbtcnVlFJSS34C3RCS8YKQkT98tn7GL1OaUcI46ySr9AxlyWRRLITNFyCD70zeA2_JvDG-S0eA17BCGbEyxhSKs4jgJ0dPybduXGPncersE2f8cLji3vdDx3g9TjZ_QytXArRQkwztob7HJPl7qALQw9-fIOOWt0lePt4n6Lbrxc3y2_F9ffLq-XiujBcyLFo6IYRqJpWmJYZKRtqtBGkNNa2vK3sRvKaWgac6401VGdTA5WNFS2XlSX8FH150B2mTQ_W5NRRd2qIrtdxr4J26tDj3U-1DXeK0rIWTVVmhY-PCjHk3qRR9S4Z6DrtIUxJcUrr3PRKNBn98A-6C1P0ub6ZEqImvK7-UlvdgXK-DTmxmUXVoqFM0LJhIlNn_6HysZDnFDy0Lv8fBBQPAWaeVoT2qUhK1Lwj6mBHMv_-eWee6D9LwX8DUty3zg</recordid><startdate>20241006</startdate><enddate>20241006</enddate><creator>de Gennaro, Luciana</creator><creator>Burgio, Matteo</creator><creator>Lacalandra, Giovanni Michele</creator><creator>Petronella, Francesco</creator><creator>L'Abbate, Alberto</creator><creator>Ravasini, Francesco</creator><creator>Trombetta, Beniamino</creator><creator>Rizzo, Annalisa</creator><creator>Ventura, Mario</creator><creator>Cicirelli, Vincenzo</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2792-8848</orcidid><orcidid>https://orcid.org/0000-0002-2688-0056</orcidid><orcidid>https://orcid.org/0009-0007-9572-7630</orcidid><orcidid>https://orcid.org/0000-0002-5995-2001</orcidid><orcidid>https://orcid.org/0000-0001-7762-8777</orcidid><orcidid>https://orcid.org/0000-0002-8203-4540</orcidid><orcidid>https://orcid.org/0000-0001-9109-3561</orcidid><orcidid>https://orcid.org/0000-0003-2866-5533</orcidid></search><sort><creationdate>20241006</creationdate><title>Genomic Sequencing to Detect Cross-Breeding Quality in Dogs: An Example Studying Disorders in Sexual Development</title><author>de Gennaro, Luciana ; Burgio, Matteo ; Lacalandra, Giovanni Michele ; Petronella, Francesco ; L'Abbate, Alberto ; Ravasini, Francesco ; Trombetta, Beniamino ; Rizzo, Annalisa ; Ventura, Mario ; Cicirelli, Vincenzo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-81b20e58f6cf2c9981cac604cddf3f5db9371d2e33abdc1a937ae198d6f395d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Breeding</topic><topic>Causes of</topic><topic>Disorders of Sex Development - genetics</topic><topic>Disorders of Sex Development - veterinary</topic><topic>DNA sequencing</topic><topic>Dog breeding</topic><topic>Dog Diseases - genetics</topic><topic>Dogs</topic><topic>Female</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genome</topic><topic>Genomes</topic><topic>Genomics - methods</topic><topic>High-Throughput Nucleotide Sequencing</topic><topic>Male</topic><topic>Methods</topic><topic>Mitochondrial DNA</topic><topic>Mutation</topic><topic>Nucleotide sequencing</topic><topic>Penis</topic><topic>Phenotype</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Pseudohermaphroditism</topic><topic>Sex chromosomes</topic><topic>Sex differentiation disorders</topic><topic>X chromosomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Gennaro, Luciana</creatorcontrib><creatorcontrib>Burgio, Matteo</creatorcontrib><creatorcontrib>Lacalandra, Giovanni Michele</creatorcontrib><creatorcontrib>Petronella, Francesco</creatorcontrib><creatorcontrib>L'Abbate, Alberto</creatorcontrib><creatorcontrib>Ravasini, Francesco</creatorcontrib><creatorcontrib>Trombetta, Beniamino</creatorcontrib><creatorcontrib>Rizzo, Annalisa</creatorcontrib><creatorcontrib>Ventura, Mario</creatorcontrib><creatorcontrib>Cicirelli, Vincenzo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Gennaro, Luciana</au><au>Burgio, Matteo</au><au>Lacalandra, Giovanni Michele</au><au>Petronella, Francesco</au><au>L'Abbate, Alberto</au><au>Ravasini, Francesco</au><au>Trombetta, Beniamino</au><au>Rizzo, Annalisa</au><au>Ventura, Mario</au><au>Cicirelli, Vincenzo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genomic Sequencing to Detect Cross-Breeding Quality in Dogs: An Example Studying Disorders in Sexual Development</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2024-10-06</date><risdate>2024</risdate><volume>25</volume><issue>19</issue><spage>10763</spage><pages>10763-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Disorders of sexual development (DSDs) in dogs, similar to humans, arise from genetic mutations, gonadal differentiation, or phenotypic sex development. The French Bulldog, a breed that has seen a surge in popularity and demand, has also shown a marked increase in DSD incidence. This study aims to characterize the genetic underpinnings of DSDs in a French Bulldog named
, exhibiting ambiguous genitalia and internal sexual anatomy, and to explore the impact of breeding practices on genetic diversity within the breed. We utilized a comprehensive approach combining conventional cytogenetics, molecular techniques, and deep sequencing to investigate the genetic profile of
. The sequence data were compared to three other male French Bulldogs' genome sequences with typical reproductive anatomy, including
's father and the canine reference genome (CanFam6). We found a Robertsonian fusion involving chromosome 23 previously reported in dogs as a causative mutation responsible for sex reversal syndrome. Our findings revealed a 22% mosaicism (78,XX/77,XX), the absence of the sex-determining region (
) gene, and the presence of 43 unique Single Nucleotide Variants (SNVs) not inherited from the father. Notably, the run of homozygosity (ROH) analysis showed
has a higher number of homozygous segments compared to other Bulldogs, with a total length of these fragments 50% greater than the average, strongly suggesting this dog is the product of the mating between siblings. Although no direct causative genes for the DSD phenotype were identified, four candidate loci warrant further investigation. Our study highlighted the need for a better annotated and curated reference dog genome to define genes causative of any specific phenotype, suggests a potential genetic basis for the DSD phenotype in dogs, and underscores the consequences of uncontrolled breeding practices in French Bulldogs. These findings highlight the importance of implementing strategic genetic management to preserve genetic health and diversity in canine populations.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39409092</pmid><doi>10.3390/ijms251910763</doi><orcidid>https://orcid.org/0000-0003-2792-8848</orcidid><orcidid>https://orcid.org/0000-0002-2688-0056</orcidid><orcidid>https://orcid.org/0009-0007-9572-7630</orcidid><orcidid>https://orcid.org/0000-0002-5995-2001</orcidid><orcidid>https://orcid.org/0000-0001-7762-8777</orcidid><orcidid>https://orcid.org/0000-0002-8203-4540</orcidid><orcidid>https://orcid.org/0000-0001-9109-3561</orcidid><orcidid>https://orcid.org/0000-0003-2866-5533</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Breeding Causes of Disorders of Sex Development - genetics Disorders of Sex Development - veterinary DNA sequencing Dog breeding Dog Diseases - genetics Dogs Female Genes Genetic aspects Genome Genomes Genomics - methods High-Throughput Nucleotide Sequencing Male Methods Mitochondrial DNA Mutation Nucleotide sequencing Penis Phenotype Polymorphism, Single Nucleotide Pseudohermaphroditism Sex chromosomes Sex differentiation disorders X chromosomes |
title | Genomic Sequencing to Detect Cross-Breeding Quality in Dogs: An Example Studying Disorders in Sexual Development |
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