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Cancer Research|November 26, 1997
Loss of heterozygosity studies and deletion mapping identify two putative chromosome 14q tumor suppressor loci in renal oncocytomasR F Schwerdtle, A Winterpacht, S Störkel, et al.
Human Molecular Genetics|December 23, 1999
Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expressionD Prawitt, T Enklaar, G Klemm, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 15, 1992
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromesK Buiting, V Greger, B H Brownstein, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 30, 2018
Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2S Butscheidt, A Delsmann, T Rolvien, et al.
Osteoarthritis and Cartilage|January 21, 2020
Skeletal deterioration in COL2A1-related spondyloepiphyseal dysplasia occurs prior to osteoarthritisT Rolvien, T A Yorgan, U Kornak, et al.
American Journal of Medical Genetics|November 7, 1998
Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)T Pihlajamaa, D J Prockop, J Faber, et al.
Cytogenetics and Cell Genetics|August 31, 2001
Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene ST5) and mouse chromosome 7C Amid, A Bahr, A Mujica, et al.
American Journal of Human Genetics|September 14, 2000
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type BG C Schwabe, S Tinschert, C Buschow, et al.
Human Mutation|October 29, 1998
Ten novel mutations found in AniridiaM T Wolf, B Lorenz, A Winterpacht, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 1995
Systematic screening of an arrayed cDNA library by PCRD J Munroe, R Loebbert, E Bric, et al.
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