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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.
American Journal of Medical Genetics. Part A|January 19, 2010
Haploinsufficiency of the gene Quaking (QKI) is associated with the 6q terminal deletion syndromeLiesbeth Backx, Jean-Pierre Fryns, Carlo Marcelis, et al.
American Journal of Medical Genetics. Part A|March 23, 2012
A microdeletion proximal of the critical deletion region is associated with mild Wolf-Hirschhorn syndromeFemke Hannes, Peter Hammond, Oliver Quarrell, et al.
Prenatal Diagnosis|July 6, 2012
Cytogenetic and morphological analysis of early products of conception following hystero-embryoscopy from couples with recurrent pregnancy lossCaroline Robberecht, Anne Pexsters, Jan Deprest, et al.
International Journal of Paediatric Dentistry|December 19, 2007
The oro-dental phenotype in Prader-Willi syndrome: a survey of 15 patientsIsabelle Bailleul-Forestier, Veroniek Verhaeghe, Jean-Pierre Fryns, et al.
European Journal of Human Genetics : EJHG|July 7, 2005
Partners of mutation-carriers for Huntington's disease: forgotten persons?Marleen Decruyenaere, Gerry Evers-Kiebooms, Andrea Boogaerts, et al.
European Journal of Medical Genetics|September 24, 2005
Interstitial 6q deletion: clinical and array CGH characterisation of a new patientCédric Le Caignec, Ann Swillen, Elvire Van Asche, et al.
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