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Nature Genetics|June 1, 1993
Assignment of an autosomal sex reversal locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3-q25.1N Tommerup, W Schempp, P Meinecke, et al.
American Journal of Medical Genetics|November 15, 1993
Congenital diaphragmatic hernia in the Brachmann-de Lange syndromeC Cunniff, C J Curry, J C Carey, et al.
Clinical Genetics|August 6, 2011
Microcephalic osteodysplastic primordial dwarfism type I with biallelic mutations in the RNU4ATAC geneR Nagy, H Wang, B Albrecht, et al.
European Radiology|December 22, 1999
MR imaging of the male pelvisJ O Barentsz, M R Engelbrecht, J A Witjes, et al.
Hormone and Metabolic Research. Supplement Series|January 1, 1990
Analysis and processing of data in a hospital-based diabetes management systemK Piwernetz, R Renner, A Möhrlein, et al.
European Journal of Pediatrics|June 1, 1994
The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patientsC Schrander-Stumpel, P Meinecke, G Wilson, 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.
European Journal of Ultrasound : Official Journal of the European Federation of Societies for Ultrasound in Medicine and Biology|February 11, 1999
Follow-up of Wilms' tumour during pre-operative chemotherapy by qualitative and quantitative sonographyM R Engelbrecht, C Hitge-Boetes, J Coolen, et al.
American Journal of Medical Genetics|September 6, 1996
Isochromosome Xq in Klinefelter syndrome: report of 7 new casesS Arps, T Koske-Westphal, P Meinecke, et al.
European Radiology|August 27, 2002
Local staging of prostate cancer using magnetic resonance imaging: a meta-analysisMarc R Engelbrecht, Gerrit J Jager, Robert J Laheij, et al.
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