Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions

Human Molecular Genetics

Volumn 8, Issue 2, 1999, Pages 313-321

  Wu, Yuan Qing ^a   Heilstedt, Heidi A ^a   Bedell, Joseph A ^b,c   May, Kristin M ^d   Starkey, David E ^a   McPherson, John D ^c   Shapira, Stuart K ^a   Shaffer, Lisa G ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

ARTICLE; CHROMOSOME 1P; CHROMOSOME BREAKAGE; CLINICAL ARTICLE; CLINICAL FEATURE; EXTRACHROMOSOMAL INHERITANCE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETIC ANALYSIS; HUMAN; MALE; PHENOTYPE; PRIORITY JOURNAL;

CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 1; DNA; DNA PROBES; GENETIC MARKERS; GENOTYPE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PEDIGREE; PHENOTYPE; PHYSICAL CHROMOSOME MAPPING;

EID: 0032898935     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.2.313     Document Type: Article

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