Author:
Gajecka Marzena,Yu Wei,Ballif Blake C,Glotzbach Caron D,Bailey Kristen A,Shaw Chad A,Kashork Catherine D,Heilstedt Heidi A,Ansel David A,Theisen Aaron,Rice Ritva,Rice David P C,Shaffer Lisa G
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference70 articles.
1. Francke U : Regional localization of the human genes for malate dehydrogenase-1 and isocitrate dehydrogenase-1 on chromosome 2 by interspecific hybridization using human cells with the balanced reciprocal translocation t(1;2) (q32;q13). Cytogenet Cell Genet 1975; 14: 308–312.
2. Nickerson E, Greenberg F, Keating MT, McCaskill C, Shaffer LG : Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndrome. Am J Hum Genet 1995; 56: 1156–1165.
3. Ewart AK, Morris CA, Atkinson D et al: Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nat Genet 1993; 5: 11–16.
4. Breuning MH, Dauwerse HG, Fugazza G et al: Rubinstein–Taybi syndrome caused by submicroscopic deletions within 16p13.3. Am J Hum Genet 1993; 52: 249–254.
5. Ballabio A, Andria G : Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses. Hum Mol Genet 1992; 1: 221–227.
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