Two patients with duplication of 17p11.2: The reciprocal of the Smith-Magenis syndrome deletion?

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 63, Issue 2, 1996, Pages 373-377

  Brown, Angela ^a,b   Phelan, Mary C ^a   Patil, Shivanand ^d   Crawford, Eric ^a   Rogers, R Curtis ^a,c   Schwartz, Charles ^a,b  

^a GREENWOOD GENETIC CENTER   (United States)

^b CLEMSON UNIVERSITY   (United States)

^c GREENVILLE HOSPITAL SYSTEM   (United States)

^d UNIVERSITY OF IOWA   (United States)

Author keywords

Deletion 17p11.2; Duplication 17p11.2; Smith Magenis syndrome

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CHROMOSOME 17P; CHROMOSOME DUPLICATION; CYTOGENETICS; DEVELOPMENTAL DISORDER; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE DOSAGE; GENETIC ANALYSIS; HUMAN; MALE; PRIORITY JOURNAL; SISTER CHROMATID EXCHANGE; SMITH MAGENIS SYNDROME;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 17; FOLLOW-UP STUDIES; GENETIC MARKERS; GROWTH DISORDERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; MALE; MULTIGENE FAMILY; SYNDROME;

EID: 0029927224     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960517)63:2<373::AID-AJMG9>3.0.CO;2-U     Document Type: Article

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