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American Journal of Human Genetics|July 10, 2001
Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancyJ M Graham, K Anyane-Yeboa, A Raams, et al.American Journal of Human Genetics|March 1, 1995
Clinical and molecular characterization of patients with distal 11q deletionsL A Penny, M Dell'Aquila, M C Jones, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 22, 2011
Male sexual development in utero: testicular descent on prenatal magnetic resonance imagingS F Nemec, U Nemec, M Weber, et al.American Journal of Medical Genetics|May 1, 1989
Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndromeU Tantravahi, R D Nicholls, H Stroh, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 18, 2011
Female external genitalia on fetal magnetic resonance imagingS F Nemec, U Nemec, M Weber, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|April 13, 2011
Penile biometry on prenatal magnetic resonance imagingS F Nemec, U Nemec, M Weber, et al.American Journal of Human Genetics|January 11, 1991
Analysis of the chondroitin sulfate proteoglycan core protein (CSPGCP) gene in achondroplasia and pseudoachondroplasiaJ E Finkelstein, K Doege, Y Yamada, et al.Journal of Medical Genetics|November 1, 1996
Exclusion of candidate loci and cholesterol biosynthetic abnormalities in familial Pallister-Hall syndromeL G Biesecker, S Kang, A A Schäffer, et al.American Journal of Human Genetics|August 11, 1991
Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15J Wagstaff, J H Knoll, J Fleming, et al.American Journal of Medical Genetics|May 1, 1989
Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndromeR D Nicholls, J H Knoll, K Glatt, et al.Pageof 26