Most jacobsen syndrome deletion breakpoints occur distal to FRA11b

American Journal of Medical Genetics

Volumn 76, Issue 3, 1998, Pages 222-228

  Michaelis, R C ^a   Velagaleti, G V N ^b   Jones, C ^c   Pivnick, E K ^b   Phelan, M C ^a   Boyd, E ^e   Tarleton, J ^e   Wilroy, R S ^b   Tunnacliffe, A ^d   Tharapel, A T ^b,f  

^a GREENWOOD GENETIC CENTER   (United States)

^b UNIVERSITY OF TENNESSEE COLLEGE OF MEDICINE   (United States)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d Anglia Research Foundation   (United Kingdom)

^e Mission Genetics Center   (United States)

^f UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

11q syndrome; Fragile sites; Trinucleotide repeats

Indexed keywords

DNA;

ARTICLE; CASE REPORT; CHROMOSOME 11Q; CHROMOSOME DELETION; CHROMOSOME FRAGILE SITE; CYTOGENETICS; FEMALE; GENETIC DISORDER; HUMAN; INFANT; JACOBSEN SYNDROME; KARYOTYPE; MULTIPLE MALFORMATION SYNDROME; NERVOUS SYSTEM MALFORMATION; PRIORITY JOURNAL; SOUTHERN BLOTTING; SYNDROME DELINEATION; TRINUCLEOTIDE REPEAT;

EID: 0032546337     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980319)76:3<222::AID-AJMG5>3.0.CO;2-S     Document Type: Article

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