Familial X-linked mental retardation and isolated growth hormone deficiency: Clinical and molecular findings

American Journal of Medical Genetics

Volumn 64, Issue 1, 1996, Pages 35-41

  Hamel, Ben C J ^a   Smits, Arie P T ^a   Otten, Barto J ^a   Van Den Helm, Bellinda ^a   Ropers, Hans Hilger ^a   Mariman, Edwin C M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

gene localization; isolated growth hormone deficiency; X linked mental retardation

Indexed keywords

GROWTH HORMONE;

ADULT; ARTICLE; BEHAVIOR DISORDER; BODY HEIGHT; CHROMOSOME XQ; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENETIC LINKAGE; GROWTH HORMONE DEFICIENCY; HUMAN; MALE; MENTAL DEFICIENCY; PHENOTYPE; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER;

ADULT; AGED; CHILD; FEMALE; HETEROZYGOTE DETECTION; HUMAN GROWTH HORMONE; HUMANS; LINKAGE (GENETICS); MALE; MENTAL RETARDATION; MIDDLE AGED; PEDIGREE; X CHROMOSOME;

EID: 0029971076     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960712)64:1<35::AID-AJMG5>3.0.CO;2-Q     Document Type: Article

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