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American Journal of Medical Genetics|September 15, 1994
A variety of genetic mechanisms are associated with the Prader-Willi syndromeT Woodage, Z M Deng, M Prasad, et al.
Science (New York, N.Y.)|June 2, 1989
Two NF1 translocations map within a 600-kilobase segment of 17q11.2P O'Connell, R Leach, R M Cawthon, et al.
Genomics|September 1, 1992
The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1L R Hendricks-Taylor, L L Bachinski, M J Siciliano, et al.
American Journal of Human Genetics|May 1, 1995
Deletions of the elastin gene at 7q11.23 occur in approximately 90% of patients with Williams syndromeE Nickerson, F Greenberg, M T Keating, et al.
American Journal of Medical Genetics|April 10, 1995
De novo tandem duplication of chromosome segment 22q11-q12: clinical, cytogenetic, and molecular characterizationE A Lindsay, L G Shaffer, R Carrozzo, et al.
American Journal of Human Genetics|May 1, 1990
Molecular studies of DiGeorge syndromeW J Fibison, M Budarf, H McDermid, et al.
Somatic Cell and Molecular Genetics|July 1, 1987
Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localizationG I Liou, S L Fong, J Gosden, et al.
American Journal of Obstetrics and Gynecology|February 1, 1990
Cytogenetic results of chorionic villus sampling: high success rate and diagnostic accuracy in the United States collaborative studyD H Ledbetter, A O Martin, Y Verlinsky, et al.
American Journal of Human Genetics|November 1, 1992
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGMR A Bascom, J García-Heras, C L Hsieh, et al.
Genomics|December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN geneA Mutirangura, A Jayakumar, J S Sutcliffe, et al.
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