Molecular analysis of the Smith-Magenis syndrome: A possible contiguous- gene syndrome associated with del(17)(p11.2)

American Journal of Human Genetics

Volumn 49, Issue 6, 1991, Pages 1207-1218

  Greenberg, F ^a   Guzzetta, V ^a   De Oca Luna, R M ^a   Magenis, R E ^a   Smith, A C M ^a   Richter, S F ^a   Kondo, I ^a   Dobyns, W B ^a   Patel, P I ^a   Lupski, J R ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER;

ADULT; ARTICLE; CHILD; CHROMOSOME 17P; CLINICAL ARTICLE; DNA PROBE; FEMALE; GENOME IMPRINTING; HUMAN; HUMAN CELL; INFANT; INTERSTITIAL CHROMOSOME DELETION; MALE; PARTIAL MONOSOMY; PHENOTYPE; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME;

ADOLESCENT; ADULT; AGED; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHROMOSOME BANDING; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENETIC MARKERS; HUMAN; INFANT; MALE; MENTAL RETARDATION; MIDDLE AGE; MOLECULAR SEQUENCE DATA; PARENTS; PEDIGREE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; SYNDROME;

EID: 0026347929     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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