X-linked mental retardation with neonatal hypotonia in a French family (MRX15): Gene assignment to Xp11.22-Xp21.1

American Journal of Medical Genetics

Volumn 64, Issue 1, 1996, Pages 97-106

  Raynaud, Martine ^a   Gendrot, Chantal ^a   Dessay, Benoit ^a   Moncla, Anne ^b   Ayrault, Anne Dominique ^a   Moizard, Marie Pierre ^a   Toutain, Annick ^a   Briault, Sylvain ^a   Villard, Laurent ^c   Ronce, Nathalie ^a   Moraine, Claude ^a  

^a CHU BRETONNEAU   (France)

^b Cytogenetics Laboratory Marseille University Medical Center   (France)

^c INSERM   (France)

Author keywords

congenital hypotonia; gene mapping; linkage analysis; MRX; proximal Xp; X linked mental retardation

Indexed keywords

ADULT; ARTICLE; CHROMOSOME XP; CLINICAL ARTICLE; FEMALE; FRANCE; GENE ASSIGNMENT; GENETIC LINKAGE; GENETIC RECOMBINATION; HUMAN; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; MUSCLE HYPOTONIA; NEWBORN DISEASE; PEDIGREE ANALYSIS; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER;

ADULT; CHROMOSOME MAPPING; FACIES; FEMALE; FRANCE; HETEROZYGOTE DETECTION; HUMANS; INFANT, NEWBORN; LINKAGE (GENETICS); MALE; MENTAL RETARDATION; MUSCLE HYPOTONIA; NEUROPSYCHOLOGICAL TESTS; PEDIGREE; X CHROMOSOME;

EID: 0029887239     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960712)64:1<97::AID-AJMG17>3.0.CO;2-N     Document Type: Article

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