Mole maker phenotype: possible narrowing of the candidate region

Recent data has suggested that familial recurrent hydatidiform mole is a rare autosomal recessive trait in women experiencing this gestational disease (MIM 231090). Here we provide molecular data on an additional family confirming that recurrent familial hydatidiform moles are diploid, biparental an...

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Veröffentlicht in:European journal of human genetics : EJHG 2000-08, Vol.8 (8), p.641-644
Hauptverfasser: Sensi, A, Gualandi, F, Pittalis, M C, Calabrese, O, Falciano, F, Maestri, I, Bovicelli, L, Calzolari, E
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container_issue 8
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container_title European journal of human genetics : EJHG
container_volume 8
creator Sensi, A
Gualandi, F
Pittalis, M C
Calabrese, O
Falciano, F
Maestri, I
Bovicelli, L
Calzolari, E
description Recent data has suggested that familial recurrent hydatidiform mole is a rare autosomal recessive trait in women experiencing this gestational disease (MIM 231090). Here we provide molecular data on an additional family confirming that recurrent familial hydatidiform moles are diploid, biparental and arise from independent conceptions. A narrowing of the gene interval on chromosome 19q13.3-13.4 is suggested by haplotype analysis in two sisters.
doi_str_mv 10.1038/sj.ejhg.5200501
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source MEDLINE; EZB-FREE-00999 freely available EZB journals; SpringerLink Journals - AutoHoldings
subjects Adult
Chromosome 19
Chromosome Aberrations
Chromosome Disorders
Chromosome Mapping
Chromosomes
Chromosomes, Human, Pair 19 - genetics
Family Health
Female
Flow cytometry
Genetic Linkage
Genetics
Genomes
Haplotypes
Homozygote
Humans
Hydatidiform mole
Hydatidiform Mole - genetics
Lod Score
Male
Microsatellite Repeats
Pedigree
Phenotypes
Ploidies
Pregnancy
Recessive traits
Sequence Tagged Sites
Uterine Neoplasms - genetics
Womens health
title Mole maker phenotype: possible narrowing of the candidate region
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