Molecular mechanism for duplication 17p11.2 - The homologous recombination reciprocal of the Smith-Magenis microdeletion

Nature Genetics

Volumn 24, Issue 1, 2000, Pages 84-87

  Potocki, Lorraine ^a   Chen, Ken Shiung ^a   Park, Sung Sup ^a   Osterholm, Doreen E ^a   Withers, Marjorie A ^a   Kimonis, Virginia ^b   Summers, Anne M ^c   Meschino, Wendy S ^c   Anyane Yeboa, Kwame ^d   Kashork, Catherine D ^a   Shaffer, Lisa G ^a   Lupski, James R ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b SOUTHERN ILLINOIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c NORTH YORK GENERAL HOSPITAL   (Canada)

^d Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 17P; CLINICAL ARTICLE; FEMALE; GENE CLUSTER; GENE DELETION; GENE DUPLICATION; GENE LOCUS; GENE REARRANGEMENT; GENETIC RECOMBINATION; GENOME; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 17; FEMALE; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MENTAL RETARDATION; PEDIGREE; RECOMBINATION, GENETIC; SYNDROME;

EID: 0033987366     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/71743     Document Type: Article

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