Showing results (681-690 of 1,155) with videos related to
Sort By:
Pageof 116
Genetic Counseling (Geneva, Switzerland)|August 6, 2005
A novel Fryns "Anophthalmia-plus" syndrome associated with primary hypothyroidismI Akalin, D A Senses, H Ilgin-Ruhi, et al.Genetic Counseling (Geneva, Switzerland)|August 6, 2005
A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) familyK Fontaine, O Sémonin, J P Legarde, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
A review of 35 cases of asymmetric crying faciesH Caksen, D Odabaş, O Tuncer, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Familial cylindromatosisC Stoll, Y Alembik, A Wilk, et al.Genetic Counseling (Geneva, Switzerland)|August 4, 2004
Hereditary gingival fibromatosis and sensorineural hearing loss in a 42-year-old man with Jones syndromeO Kasaboğlu, C Tümer, S BalciGenetic Counseling (Geneva, Switzerland)|January 22, 2005
Age at diagnosis, body mass index and physical morbidity in children and adults with the Prader-Willi syndromeA Vogels, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 22, 2005
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delayC P Chen, S P Lin, S R Chern, et al.Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Complete achromatopsia associated with skeletal anomalies: a new autosomal recessive syndromeJ E García-Ortiz, D García-Cruz, R Mendoza-Topete, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Familial occurrence of unilateral biphalangeal duplication of the thumbL De Smet, G FabryGenetic Counseling (Geneva, Switzerland)|April 23, 2005
A natural history of a child with monosomy 5p syndrome (Cat-cry/Cri-du-chat syndrome) during the 18 years of follow-upR Posmyk, B Panasiuk, S A Yatsenko, et al.Pageof 116