Regional Localization of an X-Linked Mental Retardation Gene to Xp21.1-Xp22.13 (MRX38)

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 64, Issue 1, 1996, Pages 89-96

  Schutz, Christopher K ^a   Ives, Elizabeth J ^b   Chalifoux, Maryse ^d   MacLaren, Linda ^b   Farrell, Sandra ^e   Robinson, Paula D ^a   White, Bradley N ^a   Holden, Jeanette J A ^c,d  

^a MCMASTER UNIVERSITY   (Canada)

^b New Janeway Childrens Health and Rehabilitation Centre   (Canada)

^c QUEEN S UNIVERSITY   (Canada)

^d Ongwanada Resource Centre   (Canada)

^e CREDIT VALLEY HOSPITAL   (Canada)

Author keywords

Macrocephaly; MRX38; Seizures; X linked mental retardation; XLMR; Xp21.1 Xp22.13

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME XP; FEMALE; GENE LOCATION; GENETIC RECOMBINATION; HUMAN; MAJOR CLINICAL STUDY; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PEDIGREE ANALYSIS; PRIORITY JOURNAL; X CHROMOSOME LINKED DISORDER;

ADOLESCENT; ADULT; BRAIN; CHROMOSOME MAPPING; FEMALE; HUMANS; LINKAGE (GENETICS); MALE; MENTAL RETARDATION; PEDIGREE; RECOMBINATION, GENETIC; SEIZURES; X CHROMOSOME;

EID: 0029891633     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960712)64:1<89::AID-AJMG16>3.0.CO;2-O     Document Type: Article

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