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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.
American Journal of Medical Genetics. Part A|March 1, 2005
Carpal and tarsal synostoses and transverse reduction defects of the toes in two brothers heterozygous for a double de novo NOGGIN mutationPhilippe Debeer, Christel Huysmans, Wim J M Van de Ven, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|September 23, 2006
Pseudomyxoma peritonei associated with a mucinous ovarian tumor arising from a mature cystic teratoma. A case reportSophie Marquette, Frederic Amant, Ignace Vergote, et al.
Autism : the International Journal of Research and Practice|May 29, 2004
Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autismDries Castermans, Valérie Wilquet, Jean Steyaert, et al.
American Journal of Medical Genetics|March 29, 2002
Glypican 1 gene: good candidate for brachydactyly type EMaria Syrrou, Katelÿne Keymolen, Koen Devriendt, et al.
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