Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry

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Bibliographic Details
Published in:	Journal of medical genetics Vol. 37; no. 10; pp. 804 - 807
Main Authors:	SCHMIDT, HEINRICH, UHRIG, SABINE, LEDERER, GABY, MURKEN, JAN, SPEICHER, MICHAEL R, SCHUFFENHAUER, SIMONE
Format:	Journal Article
Language:	English
Published:	England BMJ Publishing Group Ltd 01-10-2000 BMJ Publishing Group LTD BMJ Group
Subjects:	Abnormalities, Multiple - genetics Adult Child Child, Preschool Chromosome Banding Chromosome Breakage - genetics Chromosome Deletion Chromosomes, Artificial, Yeast Chromosomes, Human, Pair 12 - genetics Chromosomes, Human, Pair 7 - genetics Female Fibroblasts Gene Duplication Genetic Heterogeneity Genotype Humans Hypopigmentation - genetics In Situ Hybridization, Fluorescence Infant Infant, Newborn Intellectual Disability - genetics Karyotyping Letters to the Editor Lymphocytes Male Mosaicism - genetics Phenotype Trisomy - genetics
Online Access:	Get full text
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Bibliography:	href:jmedgenet-37-804.pdf PMID:11183189 local:jmedgenet;37/10/804 ark:/67375/NVC-R62HN7QW-P istex:0532CE4C52219E2F87244183955EA36D23940AF7
ISSN:	0022-2593 1468-6244 1468-6244
DOI:	10.1136/jmg.37.10.804