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Annales De Genetique|April 6, 2002
Atypical presentation of the Prader-Willi syndrome. Mosaic trisomy 15?Annick Vogels, Maureen Holvoet, Mie-Jef Descheemaeker, et al.
International Journal of Surgical Pathology|April 22, 2016
Mesonephric (Wolffian) Pseudoendometrioid Carcinoma of the Broad Ligament, Arising From a Papillary CystadenomaPhilippe Moerman, Frederic Amant, Ignace Vergote
The Journal of Clinical Endocrinology and Metabolism|June 6, 2003
Genetic and phenotypic heterogeneity in patients with mandibuloacral dysplasia-associated lipodystrophyVinaya Simha, Anil K Agarwal, Elif Arioglu Oral, et al.
Twin Research : the Official Journal of the International Society for Twin Studies|January 23, 2003
The East Flanders Prospective Twin Survey (EFPTS)Catherine Derom, Robert Vlietinck, Evert Thiery, et al.
European Journal of Pediatrics|March 21, 2007
What's new in karyotyping? The move towards array comparative genomic hybridisation (CGH)Thomy J L de Ravel, Koen Devriendt, Jean-Pierre Fryns, et al.
The Journal of Clinical Endocrinology and Metabolism|November 10, 2005
A homozygous mutation in the lamin A/C gene associated with a novel syndrome of arthropathy, tendinous calcinosis, and progeroid featuresHilde Van Esch, Anil K Agarwal, Philippe Debeer, et al.
American Journal of Medical Genetics|October 12, 2002
Clinical study and haplotype analysis in two brothers with Partington syndromeSuzanna G M Frints, Martine Borghgraef, Guy Froyen, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
A dysmorphic boy with 4qter deletion and 4q32.3-34.3 duplication: clinical, cytogenetic, and molecular findingsGriet Van Buggenhout, Nicole M C Maas, Jean-Pierre Fryns, et al.
Acta Oto-Laryngologica|June 24, 2008
Audiological outcomes after cochlear implantation in a patient with Melnick-Needles syndromeAnnelies Vermeiren, Andrzej Zarowski, Jean-Pierre Fryns, et al.
American Journal of Medical Genetics. Part A|March 29, 2005
Acrofacial dysostosis type RodríguezBoyan Dimitrov, Irina Balikova, Nely Jekova, et al.
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