Showing results (1451-1460 of 7,182) with videos related to
Sort By:
Pageof 719
Clinical Genetics|June 1, 1978
Familial occurrence of lumbar spondylolysis and spondylolisthesisK Haukipuro, N Keränen, E Koivisto, et al.Clinical Genetics|April 1, 1984
Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findingsT Reed, M G ButlerClinical Genetics|September 1, 1983
Frontonasal dysplasia, coronal craniosynostosis, pre- and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and variable expression?M L Kwee, D LindhoutClinical Genetics|September 1, 1980
Sialidosis type 2 (acid neuraminidase deficiency): clinical and biochemical features of a further caseR M Winter, D M Swallow, M Baraitser, et al.Clinical Genetics|September 1, 1980
A modified method for the identification of heterozygotes for Gaucher's disease using differential thermal inactivationC Goodman, J S O'BrienClinical Genetics|July 1, 1978
Presymptomatic diagnosis of adult onset polycystic kidney disease by ultrasonographyB Wolf, A T Rosenfield, K J Taylor, et al.Clinical Genetics|July 1, 1978
H-Y antigen in human intersexualityS N Ghosh, P N Shah, H M Gharpure, et al.Clinical Genetics|July 1, 1978
Charcot-Marie-Tooth disease: data for genetic counseling relating age to riskT D Bird, G H KraftClinical Genetics|August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six familiesJ M Vance, P M Conneally, R S Wappner, et al.Clinical Genetics|August 1, 1981
Multiple forms of membrane-bound beta-glucosidase in Gaucher's diseaseM Yaqoob, M CarrollPageof 719