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Genetic Counseling (Geneva, Switzerland)|August 6, 2005
MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literatureL Garavelli, K Leask, C Zanacca, et al.Genetic Counseling (Geneva, Switzerland)|August 6, 2005
Familial transmission of a dysmorphic syndrome: a variant example of Kabuki syndrome?V Belengeanu, K Rozsnyai, S Farcaş, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
The role of the Y-chromosome in sex determinationT Lukusa, J P Fryns, H van der BergheGenetic Counseling (Geneva, Switzerland)|January 1, 1994
The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual familiesC Schrander-Stumpel, H Meyer, D Merckx, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Terminal deletion of the short arm of chromosome 3L A Lizcano-Gil, L E FigueraGenetic Counseling (Geneva, Switzerland)|January 1, 1994
LADD syndrome in five members of a three-generation family and prenatal diagnosisC Francannet, P Vanlieferinghen, P Dechelotte, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
Familial Sotos syndrome: longitudinal study of two additional casesP Scarpa, R Faggioli, A VoghenziGenetic Counseling (Geneva, Switzerland)|January 1, 1994
Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boyS Tuffery, P Moine, P Sarda, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1994
The Prader-Willi syndrome: a self supporting program for children, youngsters and adultsM J Descheemaeker, A Swillen, L Plissart, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Familial cystic hygroma. Report of 8 cases in 3 familiesJ Tricoire, M F Sarramon, M Rolland, et al.Pageof 116