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S L Sklower

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Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1983
Acid alpha-glucosidase deficiency in cultured fibroblasts with phenotype 2 of acid alpha-glucosidaseN G Beratis, L Wilbur, S L Sklower
Clinical Genetics|February 1, 1986
Sanfilippo disease in GreeceN G Beratis, S L Sklower, L Wilbur, et al.
Clinical Genetics|July 1, 1989
Angiokeratoma corporis diffusum in GM1 gangliosidosis, type 1N G Beratis, A Varvarigou-Frimas, S Beratis, et al.
American Journal of Medical Genetics. Supplement|January 1, 1988
Oligosaccharyl diphosphodolichols in the ceroid-lipofuscinosesR K Pullarkat, K S Kim, S L Sklower, et al.
Pediatric Neurology|November 1, 1986
Farber lipogranulomatosis: an unusual presentation in a black childL Eviatar, S L Sklower, K Wisniewski, et al.
American Journal of Medical Genetics|January 1, 1986
Variability of thymidylate synthase activity in whole blood cultures treated with FUdRS L Sklower, E C Jenkins, M L Anderson, et al.
Clinical Genetics|September 11, 1992
Reassessment of a chromosome 12q+ marker by fluorescent in situ hybridization (FISH)A Jeziorowska, G E Houck, X L Yao, et al.
Clinical Genetics|February 1, 1989
Chromosomal abnormalities in amniotic fluid cell cultures: a comparison of apparent pseudomosaicism in Chang and RPMI-1640 mediaM S Krawczun, E C Jenkins, A Masia, et al.
Human Genetics|April 1, 1987
Further evidence for genetic heterogeneity in the fragile X syndromeW T Brown, E C Jenkins, A C Gross, et al.
Human Genetics|January 1, 1984
Distal duplication 14q: report of three cases and further delineation of the syndromeS L Sklower, E C Jenkins, S L Nolin, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 31, 1983
Acid alpha-glucosidase deficiency in cultured fibroblasts with phenotype 2 of acid alpha-glucosidaseN G Beratis, L Wilbur, S L Sklower
Clinical Genetics|February 1, 1986
Sanfilippo disease in GreeceN G Beratis, S L Sklower, L Wilbur, et al.
Clinical Genetics|July 1, 1989
Angiokeratoma corporis diffusum in GM1 gangliosidosis, type 1N G Beratis, A Varvarigou-Frimas, S Beratis, et al.
American Journal of Medical Genetics. Supplement|January 1, 1988
Oligosaccharyl diphosphodolichols in the ceroid-lipofuscinosesR K Pullarkat, K S Kim, S L Sklower, et al.
Pediatric Neurology|November 1, 1986
Farber lipogranulomatosis: an unusual presentation in a black childL Eviatar, S L Sklower, K Wisniewski, et al.
American Journal of Medical Genetics|January 1, 1986
Variability of thymidylate synthase activity in whole blood cultures treated with FUdRS L Sklower, E C Jenkins, M L Anderson, et al.
Clinical Genetics|September 11, 1992
Reassessment of a chromosome 12q+ marker by fluorescent in situ hybridization (FISH)A Jeziorowska, G E Houck, X L Yao, et al.
Clinical Genetics|February 1, 1989
Chromosomal abnormalities in amniotic fluid cell cultures: a comparison of apparent pseudomosaicism in Chang and RPMI-1640 mediaM S Krawczun, E C Jenkins, A Masia, et al.
Human Genetics|April 1, 1987
Further evidence for genetic heterogeneity in the fragile X syndromeW T Brown, E C Jenkins, A C Gross, et al.
Human Genetics|January 1, 1984
Distal duplication 14q: report of three cases and further delineation of the syndromeS L Sklower, E C Jenkins, S L Nolin, et al.
Pageof 2