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Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Cytogenetic findings in a consecutive series of 478 patients with Turner syndrome. The Leuven experience 1965-1989A Kleczkowska, E Dmoch, E Kubien, et al.Genetic Counseling (Geneva, Switzerland)|October 23, 2010
A male newborn infant with fatco syndrome (fibular aplasia, tibial campomelia and oligodactyly): a case reportA Karaman, H KahveciGenetic Counseling (Geneva, Switzerland)|October 23, 2010
An uncommon association of vacterl complex with hypertrophic pyloric stenosis and horseshoe lungM S Ipek, A Zenciroglu, M Aydin, et al.Genetic Counseling (Geneva, Switzerland)|October 23, 2010
Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouthS Balci, B Yuksel Konuk, F Atik, et al.Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Aplasia cutis congenita associated with Goltz syndrome in a male neonateD K Gnamey, K S Koffi, K Nagalo, et al.Genetic Counseling (Geneva, Switzerland)|August 5, 2009
A novel loss-of-function mutation in the GNS gene causes Sanfilippo syndrome type DN H Elçioglu, B Pawlik, B Colak, et al.Genetic Counseling (Geneva, Switzerland)|August 5, 2009
A Turkish newborn infant with cerebellar agenesis/neonatal diabetes mellitus and PTF1A mutationE Tutak, M Satar, H Yapicioğlu, et al.Genetic Counseling (Geneva, Switzerland)|August 5, 2009
Unilateral microtia in an infant with trisomy 18 mosaicismE Giannatou, H Leze, A Katana, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Revisiting foundations of autonomy and beneficence in genetic counselingV E HeadingsGenetic Counseling (Geneva, Switzerland)|January 1, 1997
A new case of Pfeiffer syndrome with mutation in FGFR2M C Addor, F Gudinchet, R N Laurini, et al.Pageof 116