Precise localisation of 3p25 breakpoints in four patients with the 3p- syndrome

Journal of Medical Genetics

Volumn 33, Issue 10, 1996, Pages 842-847

  Drumheller, Timothy ^a   McGillivray, Barbara C ^b   Behrner, Diana ^c   MacLeod, Patrick ^b   McFadden, Deborah E ^b   Roberson, Jacquelyn ^d   Venditti, Charles ^e   Chorney, Karen ^e   Chorney, Michael ^e   Smith, David I ^a  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b BC CHILDREN S HOSPITAL   (Canada)

^c Thompson Okanagan Genetic OP   (Canada)

^d HENRY FORD HOSPITAL   (United States)

^e PENN STATE COLLEGE OF MEDICINE   (United States)

Author keywords

3p syndrome; 3p25 breakpoints

Indexed keywords

DNA MARKER; MICROSATELLITE DNA;

ARTICLE; CASE REPORT; CHROMOSOME 3P; CHROMOSOME BREAKAGE; CLINICAL FEATURE; ENDOCARDIAL CUSHION DEFECT; EPSTEIN BARR VIRUS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MAPPING; GROWTH DISORDER; HUMAN; HUMAN CELL; HYBRID CELL; LYMPHOBLAST; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE; VIRUS CELL TRANSFORMATION; VON HIPPEL LINDAU DISEASE; YEAST ARTIFICIAL CHROMOSOME;

HUMAN HERPESVIRUS 4;

EID: 19244361886     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.33.10.842     Document Type: Article

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