Carpenter-Waziri syndrome results from a mutation in XNP [3]

American Journal of Medical Genetics

Volumn 85, Issue 3, 1999, Pages 249-251

  Abidi, F ^a   Schwartz, C E ^a   Carpenter, N J ^a   Villard, L ^a   Fontes, M ^a   Curtis, M ^a  

^a GREENWOOD GENETIC CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL ARTICLE; FACIES; FEMALE; GENE INACTIVATION; GENE LOCATION; GENE MAPPING; GENE MUTATION; HUMAN; LETTER; MALE; MENTAL DEFICIENCY; PEDIGREE ANALYSIS; PHENOTYPE; PHYSICAL DEVELOPMENT; PREVALENCE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SYNDROME DELINEATION; X CHROMOSOME LINKED DISORDER;

ALPHA-THALASSEMIA; AMINO ACID SEQUENCE; DNA HELICASES; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HUMANS; MALE; MENTAL RETARDATION; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; NUCLEAR PROTEINS; PEDIGREE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SYNDROME;

EID: 0033031537     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990730)85:3<249::AID-AJMG12>3.0.CO;2-U     Document Type: Letter

References (18)