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Genomics|November 1, 1991
The region of common allelic losses in sporadic renal cell carcinoma is bordered by the loci D3S2 and THRBA H van der Hout, P van der Vlies, C Wijmenga, et al.
Journal of Breath Research|February 1, 2017
Factors that influence the volatile organic compound content in human breathL Blanchet, A Smolinska, A Baranska, et al.
American Journal of Human Genetics|January 1, 1995
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesM Zatz, S K Marie, M R Passos-Bueno, et al.
Diabetologia|October 13, 2006
Association of variants of transcription factor 7-like 2 (TCF7L2) with susceptibility to type 2 diabetes in the Dutch Breda cohortJ V van Vliet-Ostaptchouk, R Shiri-Sverdlov, A Zhernakova, et al.
American Journal of Human Genetics|August 1, 1992
Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortiumM Sarfarazi, C Wijmenga, M Upadhyaya, et al.
Muscle & Nerve. Supplement|April 12, 2013
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Muscle & Nerve. Supplement|January 1, 1995
The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qterE Bakker, C Wijmenga, R H Vossen, et al.
Human Genetics|October 1, 1994
Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)S Cacurri, G Deidda, N Piazzo, et al.
Genomics|January 1, 1994
Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletionsC Wijmenga, J C van Deutekom, J E Hewitt, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 20, 2000
Refined genetic and comparative physical mapping of the canine copper toxicosis locusB van de Sluis, S Kole, M van Wolferen, et al.
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