Evidence for a new X-linked mental retardation gene in Xp21-Xp22: Clinical and molecular data in one family

American Journal of Medical Genetics

Volumn 83, Issue 2, 1999, Pages 132-137

  Ronce, Nathalie ^a   Raynaud, Martine ^a   Toutain, Annick ^a   Moizard, Marie Pierre ^a   Colleaux, Laurence ^b   Gendrot, Chantal ^a   Briault, Sylvain ^a   Moraine, Claude ^a  

^a CHU BRETONNEAU   (France)

^b INSERM   (France)

Author keywords

DP140; GK fetal brain transcript; Linkage analysis; Neonatal hypotonia; Seizures; X linked mental retardation

Indexed keywords

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 10P; CLINICAL GENETICS; DNA POLYMORPHISM; FAMILY STUDY; FEMALE; FRANCE; GENE LOCUS; GENETIC LINKAGE; HUMAN; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; MOLECULAR GENETICS; MUSCLE HYPOTONIA; PEDIGREE; PRIORITY JOURNAL;

ADULT; CHILD; CHROMOSOME MAPPING; CYTOGENETICS; DYSTROPHIN; FACE; FEMALE; GLYCEROL KINASE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MENTAL RETARDATION; MUSCLE HYPOTONIA; PEDIGREE; PROTEIN KINASES; RIBOSOMAL PROTEIN S6 KINASES, 90-KDA; SEIZURES; SYNDROME; X CHROMOSOME;

EID: 0033548696     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990312)83:2<132::AID-AJMG9>3.0.CO;2-Y     Document Type: Article

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