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Genetic Counseling (Geneva, Switzerland)|October 18, 2012
A case of onycotricodysplasia with intellectual disability, without neutropeniaM Ikbal, H K Eker, T Tos, et al.Genetic Counseling (Geneva, Switzerland)|October 18, 2012
Congenital mirror hand deformityS Arayici, G Kadioglu Simsek, M Y Oncel, et al.Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Tuberous sclerosis: clinical evaluation in a family and implications for genetic counselingN Elçioğlu, G Karatekin, M Elçioğlu, et al.Genetic Counseling (Geneva, Switzerland)|March 26, 2015
Glycogen storage disease type 1b: an early onset severe phenotype associated with a novel mutation (IVS4) in the glucose 6-phosphate translocase (SLC37A4) gene in a Turkish patientM M Oguz, E Aykan, G Yilmaz, et al.Genetic Counseling (Geneva, Switzerland)|March 26, 2015
A patient with duplication (7)(p15.3p22.3) and deletion (7)(p22.3pter) characterized by array-CGHB B Geckinli, H Aydin, A KaramanGenetic Counseling (Geneva, Switzerland)|March 26, 2015
Results of fifteen-year follow-up from a single center: findings and risks for tumor development in isolated hemihyperplasia casesT Atik, O Cogulu, F OzkinayGenetic Counseling (Geneva, Switzerland)|March 26, 2015
A male newborn with Simpson-Golabi-Behmel syndrome, presenting with metopic synostosis, anal atresia, and total anomalous pulmonary venous returnN Demir, E Peker, I Ece, et al.Genetic Counseling (Geneva, Switzerland)|January 13, 2000
A three generations family with blepharo-naso-facial malformations suggestive of Pashayan syndromeC Stoll, J Terzic, M FischbachGenetic Counseling (Geneva, Switzerland)|August 11, 2012
Bartsocas-Papas syndrome with variable expressivity in an Egyptian familyM S Zaki, A K Kamel, L K Effat, et al.Genetic Counseling (Geneva, Switzerland)|May 23, 2007
First report of a patient with a mixoploidy 47,XXX/94,XXXXXXG Rodríguez Criado, E Galán Gómez, E F Tizzano, et al.Pageof 116