X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between Xq21.33 and Xq23

American Journal of Medical Genetics

Volumn 85, Issue 3, 1999, Pages 255-262

  Chudley, Albert E ^a,b   Tackels, D C ^c   Lubs, Herbert A ^d   Arena, J Fernando ^d   Stoeber, Wendi P ^a   Kovnats, Sylvia ^a   Stevenson, Roger E ^c   Schwartz, Charles E ^c  

^a UNIVERSITY OF MANITOBA   (Canada)

^b CHILDREN S HOSPITAL RESEARCH INSTITUTE OF MANITOBA   (Canada)

^c GREENWOOD GENETIC CENTER   (United States)

^d UNIVERSITY OF MIAMI   (United States)

Author keywords

Gait disturbance; Gene mapping; Hypogammaglobulinemia; IgA deficiency; Seizures; X linked mental retardation

Indexed keywords

ARTICLE; CEREBELLUM ATROPHY; CHROMOSOME XP; CHROMOSOME XQ; CLINICAL ARTICLE; FACIES; FEMALE; GAIT DISORDER; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; HIRSUTISM; HUMAN; HYPOGAMMAGLOBULINEMIA; MALE; MENTAL DEFICIENCY; NERVE CONDUCTION; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; PROGNATHIA; SEIZURE; X CHROMOSOME LINKED DISORDER;

ABNORMALITIES, MULTIPLE; ADULT; AGAMMAGLOBULINEMIA; CHROMOSOME MAPPING; DNA; FAMILY HEALTH; FEMALE; GAIT; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MENTAL RETARDATION; MICROSATELLITE REPEATS; MIDDLE AGED; PEDIGREE; SEIZURES; SYNDROME; X CHROMOSOME;

EID: 0033039576     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990730)85:3<255::AID-AJMG14>3.0.CO;2-Z     Document Type: Article

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