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M Lubinsky

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American Journal of Medical Genetics. Supplement|January 1, 1987
Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported casesA V Moorthy, R W Chesney, M Lubinsky
American Journal of Medical Genetics|January 1, 1983
Familial amniotic bandsM Lubinsky, E Sujansky, W Sanger, et al.
Lancet (London, England)|May 11, 1974
Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndromeM Lubinsky, J Herrmann, A L Kosseff, et al.
American Journal of Medical Genetics|February 1, 1985
Syndrome of amelogenesis imperfecta, nephrocalcinosis, impaired renal concentration, and possible abnormality of calcium metabolismM Lubinsky, C Angle, P W Marsh, et al.
Pediatrics|May 1, 1984
Further delineation of the 10p deletion syndromeC L Elstner, J C Carey, G Livingston, et al.
American Journal of Medical Genetics|September 1, 1987
Familial Prader-Willi syndrome with apparently normal chromosomesM Lubinsky, H Zellweger, L Greenswag, et al.
European Journal of Pediatrics|October 1, 1976
Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 casesA L Kosseff, J Herrmann, E F Gilbert, et al.
Pediatrics|October 1, 1983
Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile typeR E Stevenson, M Lubinsky, H A Taylor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Minimum guidelines for the delivery of prenatal genetics services. The evaluation of clinical services subcommittee, Great Lakes Regional Genetics GroupA Sommer, M Lubinsky, M Cichon, et al.
American Journal of Human Genetics|October 1, 1989
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21D E Merry, J G Lesko, D M Sosnoski, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Supplement|January 1, 1987
Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported casesA V Moorthy, R W Chesney, M Lubinsky
American Journal of Medical Genetics|January 1, 1983
Familial amniotic bandsM Lubinsky, E Sujansky, W Sanger, et al.
Lancet (London, England)|May 11, 1974
Letter: Autosomal-dominant sex-dependent transmission of the Wiedemann-Beckwith syndromeM Lubinsky, J Herrmann, A L Kosseff, et al.
American Journal of Medical Genetics|February 1, 1985
Syndrome of amelogenesis imperfecta, nephrocalcinosis, impaired renal concentration, and possible abnormality of calcium metabolismM Lubinsky, C Angle, P W Marsh, et al.
Pediatrics|May 1, 1984
Further delineation of the 10p deletion syndromeC L Elstner, J C Carey, G Livingston, et al.
American Journal of Medical Genetics|September 1, 1987
Familial Prader-Willi syndrome with apparently normal chromosomesM Lubinsky, H Zellweger, L Greenswag, et al.
European Journal of Pediatrics|October 1, 1976
Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 casesA L Kosseff, J Herrmann, E F Gilbert, et al.
Pediatrics|October 1, 1983
Sialic acid storage disease with sialuria: clinical and biochemical features in the severe infantile typeR E Stevenson, M Lubinsky, H A Taylor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Minimum guidelines for the delivery of prenatal genetics services. The evaluation of clinical services subcommittee, Great Lakes Regional Genetics GroupA Sommer, M Lubinsky, M Cichon, et al.
American Journal of Human Genetics|October 1, 1989
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21D E Merry, J G Lesko, D M Sosnoski, et al.
Pageof 3