Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18

American Journal of Human Genetics

Volumn 55, Issue 3, 1994, Pages 476-483

  Boghosian Sell, L ^a   Mewar, R ^a   Harrison, W ^a   Shapiro, R M ^a   Zackai, E H ^a   Carey, J ^a   Davis Keppen, L ^a   Hudgins, L ^a   Overhauser, J ^a  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 18Q; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; EDWARDS SYNDROME; FEMALE; GENE MAPPING; HUMAN; HUMAN CELL; INFANT; MALE; MENTAL DEFICIENCY; NEWBORN; PRIORITY JOURNAL; TRISOMY 18;

ABNORMALITIES, MULTIPLE; ADULT; CASE REPORT; CELL LINE; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 18; DNA MUTATIONAL ANALYSIS; FEMALE; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; KARYOTYPING; MALE; MENTAL RETARDATION; PHENOTYPE; SUPPORT, U.S. GOV'T, P.H.S.; SYNDROME; TRISOMY;

EID: 0028037960     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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