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Journal of Medical Genetics|December 1, 1996
Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X familyB B de Vries, C C Jansen, A A Duits, et al.Journal of Medical Genetics|April 4, 2000
An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of ItoB H Eussen, G Bartalini, L Bakker, et al.Human Genetics|June 1, 1990
Paracentric inversion inv(11)(q21q23) in The NetherlandsK Madan, M H Pieters, L P Kuyt, et al.Human Reproduction (Oxford, England)|April 1, 1997
Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injectionD Van Opstal, F J Los, S Ramlakhan, et al.The Journal of Urology|March 21, 2001
Etiological studies of severe or familial hypospadiasA L Boehmer, R J Nijman, B A Lammers, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experienceJ H Tuerlings, H F de France, A Hamers, et al.Human Genetics|May 1, 1995
DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63)A M van den Ouweland, M N van der Est, E Wesby-van Swaay, et al.American Journal of Human Genetics|April 25, 2000
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromereP E Warburton, M Dolled, R Mahmood, et al.Pageof 4