Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2

Human Genetics

Volumn 110, Issue 4, 2002, Pages 366-370

  Faivre, Laurence ^a   Mégarbané, André ^b   Alswaid, Abdulrahman ^c   Zylberberg, Louise ^d   Aldohayan, Noura ^c   Campos Xavier, Ana Belinda ^a   Bacq, Delphine ^e   Legeai Mallet, Laurence ^a   Bonaventure, Jacky ^a   Munnich, Arnold ^a   Cormier Daire, Valérie ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b SAINT JOSEPH UNIVERSITY   (Lebanon)

^c The General Directorate of Armed Forces Health Services   (Saudi Arabia)

^d CNRS   (France)

^e CENTRE NATIONAL DE GÉNOTYPAGE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BRACHYDACTYLY; CHROMOSOME 19P; CHROMOSOME 19P13.3-P13.2; CONSANGUINITY; ECTOPIA LENTIS; EYE MALFORMATION; FAMILY; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; GLAUCOMA; HOMOZYGOSITY; HUMAN; JOINT STIFFNESS; LEBANON; MALE; MICROSPHEROPHAKIA; PRIORITY JOURNAL; SAUDI ARABIA; SHORT STATURE; WEILL MARCHESANI SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 19; FEMALE; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); MALE; PEDIGREE; SYNDROME;

EID: 0036556307     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-002-0689-3     Document Type: Article

References (13)

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