Showing results (771-780 of 1,155) with videos related to
Sort By:
Pageof 116
Genetic Counseling (Geneva, Switzerland)|August 23, 2007
Associated malformations in cases with neural tube defectsC Stoll, Y Alembik, B DottGenetic Counseling (Geneva, Switzerland)|January 1, 1991
Trichomegaly, pigmentary degeneration of the retina and growth disturbances. A probable autosomal recessive disorderM Mathieu, A Goldfarb, P Berquin, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Lobar holoprosencephaly and Xq22 deletionP Petit, P Moerman, J P FrynsGenetic Counseling (Geneva, Switzerland)|January 1, 1991
Epidemiology of diaphragmatic hernia in Languedoc-RoussillonP Sarda, P Devaux, G Lefort, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1991
Proteus syndrome in 7 patients: clinical and genetic considerationsD Lacombe, A Taieb, P Vergnes, et al.Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Prenatal diagnosis of trisomy 21: registration results from a single genetic centerI Witters, J P FrynsGenetic Counseling (Geneva, Switzerland)|July 16, 2008
Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutationC-P Chen, S-P Lin, Y-N Su, et al.Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Partial trisomy of the distal part of 10q: a report of two Egyptian casesM S Aglan, A K Kamel, N A HelmyGenetic Counseling (Geneva, Switzerland)|July 16, 2008
Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndromeK Salavoura, A Kolialexi, C Sofocleous, et al.Genetic Counseling (Geneva, Switzerland)|July 16, 2008
Sleep problems in individuals with 11q terminal deletion disorder (Jacobsen syndrome)A P H M Maas, P D Grossfeld, R Didden, et al.Pageof 116