Molecular characterization of patients with 18q23 deletions

American Journal of Human Genetics

Volumn 60, Issue 4, 1997, Pages 860-868

  Strathdee, Gordon ^a   Sutherland, Robert ^c   Jonsson, Jon J ^d   Sataloff, Robert ^b   Kohonen Corish, Maija ^e   Grady, Deborah ^c   Overhauser, Joan ^a,b  

^a THOMAS JEFFERSON UNIVERSITY   (United States)

^b THOMAS JEFFERSON UNIVERSITY   (United States)

^c LOS ALAMOS NATIONAL LABORATORY   (United States)

^d YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e Biology and Environment   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 18Q; CHROMOSOME DELETION; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; GENE MAPPING; GROWTH RETARDATION; HUMAN; HUMAN CELL; MENTAL DEFICIENCY; MIDFACE HYPOPLASIA; MOLECULAR GENETICS; MUSCLE HYPOTONIA; PHENOTYPE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADULT; CENTRAL NERVOUS SYSTEM DISEASES; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 18; CLONING, MOLECULAR; CYTOGENETICS; FACE; FEMALE; HUMANS; HYBRID CELLS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; LIMB DEFORMITIES, CONGENITAL; SYNDROME;

EID: 0030900735     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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