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Clinical Genetics|March 1, 1979
Familial occurrence of syngnathia congenita syndromeI Gassner, W Müller, H Rössler, et al.Clinical Genetics|April 1, 1985
On the paradoxically high relative prevalence of osteogenesis imperfecta type III in the black population of South AfricaP Beighton, G A VersfeldClinical Genetics|January 1, 1985
De novo t(4;5)(q3100;q2200) with del(5)(q1500q2200). Tentative delineation of a 5q monosomy syndrome and assignment of the critical segmentH Rivera, A Rolón, J Sánchez-Corona, et al.Clinical Genetics|January 1, 1985
Genetic counseling for autosomal dominant diseases with a negative family historyJ M FriedmanClinical Genetics|February 1, 1985
Oral and dental development in X chromosome aneuploidyP Farge, L Dallaire, G Albert, et al.Clinical Genetics|February 1, 1985
Effect of balanced X/autosome translocations on sexual and physical development. A personal experience in 4 patientsA Kleczkowska, J P Fryns, L Vinken, et al.Clinical Genetics|February 1, 1985
Diploid-tetraploid mosaicism in a malformed boyE Quiroz, A Orozco, F SalamancaClinical Genetics|February 1, 1985
The dysequilibrium syndrome: a study of the etiology and pathogenesisF Rasmussen, K H Gustavson, V R Sara, et al.Clinical Genetics|February 1, 1986
Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophyY Boyd, V J BuckleClinical Genetics|February 1, 1986
A family with congenital suprabulbar paresis (Worster-Drought syndrome)M A Patton, M Baraitser, E M BrettPageof 719