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Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13)Z Cetin, E Mihci, I Keser, et al.Genetic Counseling (Geneva, Switzerland)|August 11, 2012
A short rib polydactyly syndrome overlapping both lethal and nonlethal typesA Başgül Yiğiter, N Güdücü, Z N Kavak, et al.Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Does higher NORs expression affect the developmental stages of Down syndrome infants?R Eroz, M Okur, A Ozkan, et al.Genetic Counseling (Geneva, Switzerland)|August 11, 2012
A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndromeN Hakan, M Aydin, O Erdogan, et al.Genetic Counseling (Geneva, Switzerland)|August 11, 2012
A new clinical presentation associated with pontine clefting, hyperpigmentation and short stature in addition to craniofacial, cardiac and developmental anomaliesO Cogulu, B Durmaz, B Wollnik, et al.Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Structural chromosomal abnormalities in patients with mental retardation and/or multiple congenital anomalies: a new series of 24 patientsT Tos, A Karaman, A Aksoy, et al.Genetic Counseling (Geneva, Switzerland)|August 11, 2012
Molecular cytogenetic characterization of a case of primary amenorrhea with intrachromosomal triplication of the X chromosome q armZ Ocak, R SurucuGenetic Counseling (Geneva, Switzerland)|August 11, 2012
Emanuel syndrome due to unusual segregation of paternal originM S Zaki, A M Mohamed, A K Kamel, et al.Genetic Counseling (Geneva, Switzerland)|October 18, 2012
Angelman syndrome and thyroid dysfunctionC E Monterrubio-Ledezma, L Bobadilla-Morales, H J Pimentel-Gutiérrez, et al.Genetic Counseling (Geneva, Switzerland)|October 18, 2012
Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type IIIC P Chen, S P Lin, Y N Suo, et al.Pageof 116