Clinical and Molecular Characterization of Prader-Willi Syndrome von Sanjeeva, G. N., Maganthi, Madhuri, Kodishala, Himabindu, Marol, Rohit Kumar R., Kulshreshtha, Pooja S., Lorenzetto, Elisa, Kadandale, Jayarama S., Hladnik, Uros, Raghupathy, P., Bhat, Meenakshi

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Swyer Syndrome in Phenotypic Female with 46,XY Karyotype von Shetty, D Prashanth, Arumugam, Meenakshi, Kadandale, Jayarama S, Kumari, Suchetha

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Practice of Consanguinity and Unusual Cases of Inherited Familial Chromosome Abnormalities: A Case Report von Sanyal, Debarshi, Bhairi, Vidya, S Kadandale, Jayarama

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Next-Generation Sequencing Reveals Novel Mutations in X-linked Intellectual Disability von Muthusamy, Babylakshmi, Selvan, Lakshmi Dhevi N., Nguyen, Thong T., Manoj, Jesna, Stawiski, Eric W., Jaiswal, Bijay S., Wang, Weiru, Raja, Remya, Ramprasad, Vedam Laxmi, Gupta, Ravi, Murugan, Sakthivel, Kadandale, Jayarama S., Prasad, T.S. Keshava, Reddy, Kavita, Peterson, Andrew, Pandey, Akhilesh, Seshagiri, Somasekar, Girimaji, Satish Chandra, Gowda, Harsha

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Preimplantation Genetic Testing for Couples with Balanced Chromosomal Rearrangements von Shetty, Sachin, Nair, Jiny, Johnson, Jnapti, Shetty, Navya, Ajay Kumar, J, Thondehalmath, Nirmala, Ganesh, Deepanjali, Bhat, Vidyalakshmi R, Sajana, M, Anjana, R, Nayak, Rajsekhar, Gunasheela, Devika, Kadandale, Jayarama S, Shetty, Swathi

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Localization of the SRY Gene on Chromosome 3 in a Patient with Azoospermia and a Complex Karyotype 45,X/46,X,i(Y)(q10)/46,XX/ 47,XX,i(Y)(q10) von Barnabas, Linda C., Sumathy, Anbu, Indumathi, Muthuswamy A., Varma, Thankam R., Shetty, Swathi, Kadandale, Jayarama S., Kar, Bibhas

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ANALYSIS OF COMPLEX CHROMOSOMAL ABNORMALITIES IN A CASE OF MULTIPLE MYELOMA USING SPECTRAL KARYOTYPING von Govindasamy, Perumal, Kulshreshtha, Pooja S, Pandurangan, Prabu, Tarigopula, Anil, Kadandale, Jayarama S, Samuel, Chandra R

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Characterization of TTAGG telomeric repeats, their interstitial occurrence and constitutively active telomerase in the mealybug Planococcus lilacinus (Homoptera; Coccoidea) von Mohan, Kommu Naga, Rani, B. Sandya, Kulashreshta, Pooja Swaroop, Kadandale, Jayarama S

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Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report von Sivasankaran, Aswini, Srikanth, Ambika, Kulshreshtha, Pooja S., Anuradha, Deenadayalu, Kadandale, Jayarama S., Samuel, Chandra R.

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Splice, Insertion-Deletion and Nonsense Mutations that Perturb the Phenylalanine Hydroxylase Transcript Cause Phenylketonuria in India von Bashyam, Murali D., Chaudhary, Ajay K., Kiran, Manjari, Nagarajaram, Hampapathalu A., Devi, Radha Rama, Ranganath, Prajnya, Dalal, Ashwin, Bashyam, Leena, Gupta, Neerja, Kabra, Madhulika, Muranjan, Mamta, Puri, Ratna D., Verma, Ishwar C., Nampoothiri, Sheela, Kadandale, Jayarama S.

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Variation at Diabetes‐ and Obesity‐Associated Loci May Mirror Neutral Patterns of Human Population Diversity and Diabetes Prevalence in India von Raj, Srilakshmi M., Halebeedu, Pradeep, Kadandale, Jayarama S, Mirazon Lahr, Marta, Gallego Romero, Irene, Yadhav, Jamuna R., Iliescu, Mircea, Rai, Niraj, Crivellaro, Federica, Chaubey, Gyaneshwer, Villems, Richard, Thangaraj, Kumarasamy, Muniyappa, Kalappagowda, Chandra, H. Sharat, Kivisild, Toomas

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Cytogenetic, epidemiological and clinical profile of children with Down syndrome in Karnataka von Sharath, Krishnaveni, K.R., Asha, Prabha Subhash, Lakshmi, Kadandale, Jayarama S.

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CONSANGUINITY AND CHROMOSOMAL ABNORMALITIES von R, Lakshmi Prabha Subhash, D, Anupama, Kadandale, Jayarama S, Bhat, Meenakshi, K L, Harshal, M, Khizer Hussain Afroze

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GOLDENHAR SYNDROME: A CASE REPORT von Subhash, R Lakshmi Prabha, Anupama D, Bhat, Meenakshi, Kadandale, Jayarama S, K L, Harshal

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Variation at Diabetes- and Obesity-Associated Loci May Mirror Neutral Patterns of Human Population Diversity and Diabetes Prevalence in India: Variation at Diabetes- and Obesity-As... von Raj, Srilakshmi M., Halebeedu, Pradeep, Kadandale, Jayarama S, Mirazon Lahr, Marta, Gallego Romero, Irene, Yadhav, Jamuna R., Iliescu, Mircea, Rai, Niraj, Crivellaro, Federica, Chaubey, Gyaneshwer, Villems, Richard, Thangaraj, Kumarasamy, Muniyappa, Kalappagowda, Chandra, H. Sharat, Kivisild, Toomas

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Primed in situ labeling (PRINS) for evaluation of gene deletions in cancer von Tharapel, Sugandhi A., Kadandale, Jayarama S.

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Prader Willi/Angelman and DiGeorge/velocardiofacial syndrome deletions: Diagnosis by primed in situ labeling (PRINS) von Tharapel, Avirachan T., Kadandale, Jayarama S., Martens, Paula R., Wachtel, Stephen S., Wilroy Jr, R. Sid

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Localization of SRY by primed in situ labeling in XX and XY sex reversal von Kadandale, Jayarama S., Wachtel, Stephen S., Tunca, Yusuf, Wilroy Jr, R. Sid, Martens, Paula R., Tharapel, Avirachan T.

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Deletion of RBM and DAZ in azoospermia: Evaluation by PRINS von Kadandale, Jayarama S., Wachtel, Stephen S., Tunca, Yusuf, Martens, Paula R., Wilroy, R. Sid, Tharapel, Avirachan T.

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Hypomelanosis of Ito and a ‘mirror image’ whole chromosome duplication resulting in trisomy 14 mosaicism von Tunca, Yusuf, Wilroy, R.Sid, Kadandale, Jayarama S, Martens, Paula R, Gunther, Wendy M, Tharapel, Avirachan T

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