Search research articles
Contact Us
Filters
Showing results (21-30 of 34) with videos related to
Page
of 4
Sort By:
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 syndrome
D 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 locus
J 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 analysis
J 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 specimens
W 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 genes
V A Street, G Meekins, H P Lipe, et al.
American Journal of Medical Genetics
|
June 1, 1993
Mental retardation locus in Xp21 chromosome microdeletion
M 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 hypoplasia
E 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 syndrome
B 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 deletions
U Francke, J F Harper, B T Darras, et al.
Neurology
|
May 26, 2004
Novel insertional presenilin 1 mutation causing Alzheimer disease with spastic paraparesis
P Moretti, A P Lieberman, E A Wilde, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 34) with videos related to
Sort By:
Page
of 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 syndrome
D 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 locus
J 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 analysis
J 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 specimens
W 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 genes
V A Street, G Meekins, H P Lipe, et al.
American Journal of Medical Genetics
|
June 1, 1993
Mental retardation locus in Xp21 chromosome microdeletion
M 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 hypoplasia
E 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 syndrome
B 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 deletions
U Francke, J F Harper, B T Darras, et al.
Neurology
|
May 26, 2004
Novel insertional presenilin 1 mutation causing Alzheimer disease with spastic paraparesis
P Moretti, A P Lieberman, E A Wilde, et al.
Page
of 4