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Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Prenatal diagnosis of hereditary amyloidosis in a Portuguese family living in FranceG Lucotte, S Berriche, F David, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
The characteristic phenotype of distal 9q3 trisomy is due to duplication of band 9q32A Kleczkowska, J P Fryns, P Lemay, et al.
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Mosaic normal/15q11-q13 duplication associated with developmental delay but normal phenotypeE Goossens, P Decock, S Potgieter, et al.
Genetic Counseling (Geneva, Switzerland)|July 28, 1999
Roberts SC phocomelia with isolated cleft palate, thrombocytopenia, and eosinophiliaT Camlibel, H Mocan, N Kutlu, et al.
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Hypocalcemia and chromosome 22q11 microdeletionM Garabédian
Genetic Counseling (Geneva, Switzerland)|January 13, 2000
Unilateral longitudinal radial ray deficiency of the hand and metacarpal 4-5 synostosisL De Smet, K Keymolen, J P Fryns
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
Counseling dilemmas in EEC syndromeM Tekin, C Ohle, D E Johnson, et al.
Genetic Counseling (Geneva, Switzerland)|April 11, 2000
The KBG syndrome: an additional sporadic caseM Mathieu, M Helou, G Morin, et al.
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