Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1

American Journal of Human Genetics

Volumn 64, Issue 4, 1999, Pages 1119-1126

  Devriendt, Koenraad ^a,f   Matthijs, Gert ^a   Van Dael, Roeland ^a   Gewillig, Marc ^b   Eyskens, Benedicte ^b   Hjalgrim, Helle ^c   Dolmer, Brigitte ^d   McGaughran, Julie ^e   Bröndum Nielsen, Karen ^c   Marynen, Peter ^a,b   Fryns, Jean Pierre ^a   Vermeesch, Joris Robert ^a,b  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b DEPARTMENT OF PLANT SYSTEMS BIOLOGY   (Belgium)

^c JOHN F KENNEDY INSTITUTE   (Denmark)

^d HILLERØD HOSPITAL   (Denmark)

^e ST MARY S HOSPITAL   (United Kingdom)

^f CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER;

ADULT; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 8P; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; CYTOGENETICS; DNA POLYMORPHISM; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENOTYPE; HUMAN; HYPERACTIVITY; INTRAUTERINE GROWTH RETARDATION; MALE; MENTAL DEFICIENCY; MICROCEPHALY; PHENOTYPE; PRIORITY JOURNAL;

EID: 0033365295     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302330     Document Type: Article

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