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W K Seltzer

Showing results (21-30 of 34) with videos related to

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Clinical Chemistry|November 1, 1994
Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndromeD E Cole, L A Clarke, D C Riddell, et al.
Human Genetics|September 1, 1989
Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locusJ A Towbin, D R Wu, J Chamberlain, et al.
Genomics|July 1, 1990
DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysisJ A Towbin, J S Chamberlain, D R Wu, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1991
Screening for cystic fibrosis: feasibility of molecular genetic analysis of dried blood specimensW K Seltzer, F Accurso, M Z Fall, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genesV A Street, G Meekins, H P Lipe, et al.
American Journal of Medical Genetics|June 1, 1993
Mental retardation locus in Xp21 chromosome microdeletionM H Fries, R V Lebo, S A Schonberg, et al.
The Journal of Clinical Investigation|January 1, 1989
Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasiaE R McCabe, J Towbin, J Chamberlain, et al.
American Journal of Medical Genetics|September 1, 1988
Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndromeB A Burke, M R Wick, R King, et al.
American Journal of Human Genetics|March 1, 1987
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletionsU Francke, J F Harper, B T Darras, et al.
Neurology|May 26, 2004
Novel insertional presenilin 1 mutation causing Alzheimer disease with spastic paraparesisP Moretti, A P Lieberman, E A Wilde, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Clinical Chemistry|November 1, 1994
Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndromeD E Cole, L A Clarke, D C Riddell, et al.
Human Genetics|September 1, 1989
Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locusJ A Towbin, D R Wu, J Chamberlain, et al.
Genomics|July 1, 1990
DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysisJ A Towbin, J S Chamberlain, D R Wu, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1991
Screening for cystic fibrosis: feasibility of molecular genetic analysis of dried blood specimensW K Seltzer, F Accurso, M Z Fall, et al.
Neuromuscular Disorders : NMD|September 5, 2002
Charcot-Marie-Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genesV A Street, G Meekins, H P Lipe, et al.
American Journal of Medical Genetics|June 1, 1993
Mental retardation locus in Xp21 chromosome microdeletionM H Fries, R V Lebo, S A Schonberg, et al.
The Journal of Clinical Investigation|January 1, 1989
Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasiaE R McCabe, J Towbin, J Chamberlain, et al.
American Journal of Medical Genetics|September 1, 1988
Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndromeB A Burke, M R Wick, R King, et al.
American Journal of Human Genetics|March 1, 1987
Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletionsU Francke, J F Harper, B T Darras, et al.
Neurology|May 26, 2004
Novel insertional presenilin 1 mutation causing Alzheimer disease with spastic paraparesisP Moretti, A P Lieberman, E A Wilde, et al.
Pageof 4