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Genetic Counseling (Geneva, Switzerland)|August 19, 2011
Aniridia phenotype and myopia in a turkish boy with a PAX6 gene mutationA O Caglayan, D RobinsonGenetic Counseling (Geneva, Switzerland)|August 19, 2011
Can fetal ultrasound result in prenatal diagnosis of Prader-Willi syndrome?B Geysenbergh, L De Catte, A VogelsGenetic Counseling (Geneva, Switzerland)|August 19, 2011
An infantile case of Zellweger syndrome presented with Kabuki-like phenotypeF Ezgu, T Eminoglu, I Okur, et al.Genetic Counseling (Geneva, Switzerland)|February 7, 2012
A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 genesA O Caglayan, S Lechno, H Gumus, et al.Genetic Counseling (Geneva, Switzerland)|February 7, 2012
Alström syndrome with acanthosis nigricans: a case report and literature reviewN Akdeniz, S Gunes Bilgili, S Aktar, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1990
The lethal multiple pterygium syndrome: a nosological approachC E de Die-Smulders, C T Schrander-Stumpel, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1990
The fetal akinesia deformation sequence. A fetopathological approachP Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1990
A retrospective study of pregnancy complications among 828 cases of arthrogryposisM J Fahy, J G HallGenetic Counseling (Geneva, Switzerland)|January 1, 1990
Angelman's syndrome and 15q11-q13 deletionJ P Fryns, A Kleczowska, P Decock, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Partners of Huntington patients: implications of the disease and opinions about predictive testing and prenatal diagnosisG Evers-Kiebooms, A Swerts, H Van Den BerghePageof 116