A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome

Human Genetics

Volumn 98, Issue 4, 1996, Pages 454-459

  Davies, Angela F ^a   Olavesen, Mark G ^a   Stephens, Richard J ^a   Davidson, Rosemarie ^b   Delneste, Daniele ^c   Van Regemorter, Nicole ^c   Vamos, Esther ^c   Flinter, Frances ^a   Abusaad, Iman ^a   Ragoussis, Jiannis ^a  

^a GUY S HOSPITAL   (United Kingdom)

^b West of Scotland Regional Genetics Service   (United Kingdom)

^c ERASME HOSPITAL   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 6; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CHROMOSOME MAP; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC DISORDER; GENETICS; HUMAN; KARYOTYPING; MALE; MENTAL DEFICIENCY; MULTIPLE MALFORMATION SYNDROME; NEWBORN; SYNDROME; YEAST ARTIFICIAL CHROMOSOME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 6; FEMALE; GENETIC DISEASES, INBORN; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; MALE; MENTAL RETARDATION; SYNDROME;

EID: 17744408980     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050239     Document Type: Article

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