Cognitive function in Coffin-Lowry syndrome

Clinical Genetics

Volumn 61, Issue 4, 2002, Pages 299-304

  Simensen, Richard J ^a   Abidi, F ^a   Collins, J S ^a   Schwartz, C E ^a   Stevenson, R E ^a  

^a GREENWOOD GENETIC CENTER   (United States)

Author keywords

Coffin Lowry syndrome; Cognitive functioning; Mental retardation; RSK2 gene; X inactivation; X linked mental retardation

Indexed keywords

GENE PRODUCT; RSK2 PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; BONE DISEASE; CAUCASIAN; CHILD; CHROMOSOME XP; CLINICAL ARTICLE; COFFIN LOWRY SYNDROME; COGNITION; COGNITIVE DEFECT; COHORT ANALYSIS; CONTROLLED STUDY; CORRELATION COEFFICIENT; CULTURAL FACTOR; DISEASE ASSOCIATION; DISEASE CARRIER; FACIES; FAMILY STUDY; FEMALE; GENE LOCATION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; INTELLIGENCE; INTELLIGENCE QUOTIENT; INTELLIGENCE TEST; MALE; MENTAL DEFICIENCY; MISSENSE MUTATION; MUSCLE HYPOTONIA; NEGRO; PATHOGENESIS; PRIORITY JOURNAL; RATING SCALE; SHORT SURVEY; SOCIAL ASPECT; SOCIOECONOMICS; X CHROMOSOME INACTIVATION; X CHROMOSOME LINKAGE;

AFRICAN AMERICANS; AFRICAN CONTINENTAL ANCESTRY GROUP; ANALYSIS OF VARIANCE; COFFIN-LOWRY SYNDROME; COGNITION DISORDERS; DOSAGE COMPENSATION, GENETIC; FEMALE; HUMANS; MALE; PEDIGREE;

EID: 0036556365     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2002.610410.x     Document Type: Short Survey

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