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Molecular Biology and Evolution|July 1, 1984
Evolution of glucagon genesL C Lopez, W H Li, M L Frazier, et al.Genomics|August 1, 1992
Resolution of the two loci for autosomal dominant aniridia, AN1 and AN2, to a single locus on chromosome 11p13L A Lyons, A Martha, H A Mintz-Hittner, et al.Blood|June 1, 1988
A myeloid-related sequence that localizes to human chromosome 8q21.1-22W M Mars, P van Tuinen, H A Drabkin, et al.American Journal of Human Genetics|January 1, 1995
WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequencesV Huff, N Jaffe, G F Saunders, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1973
125 I-labeled DNA-RNA hybrids in cytological preparationsL C Altenburg, M J Getz, W R Crain, et al.Endocrine Reviews|November 1, 1991
The human placental lactogen genes: structure, function, evolution and transcriptional regulationW H Walker, S L Fitzpatrick, H A Barrera-Saldaña, et al.The Journal of Urology|October 1, 1990
Familial renal cell carcinoma: hereditary or coincidental?A K Levinson, D E Johnson, L C Strong, et al.Ophthalmic Paediatrics and Genetics|December 1, 1991
DNA diagnosis in a family with autosomal dominant aniridiaF D Verbraak, M A Mannens, E J Redeker, et al.Anticancer Research|December 31, 1997
Transcriptional activation of the bcl-2 apoptosis suppressor gene by the paired box transcription factor PAX8S M Hewitt, S Hamada, A Monarres, et al.Nature Genetics|February 1, 1993
Genetic mosaicism in normal tissues of Wilms' tumour patientsL Y Chao, V Huff, G Tomlinson, et al.Pageof 12