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Clinical Genetics
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January 5, 2001
Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients
N Bissar-Tadmouri, Y Parman, L Boutrand, et al.
Revue Neurologique
|
December 17, 2004
[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy]
B Degos, A Echaniz-Laguna, P Latour, et al.
Human Mutation
|
October 26, 1999
Two novel mutations in the MPZ gene coding region in Charcot-Marie-Tooth type 1 patients of Turkish origin: S54P, [I30del; GVYI29ins]
N Bissar-Tadmouri, Y Gulsen-Parman, P Latour, et al.
International Journal of Legal Medicine
|
May 21, 1999
Mutation of the repeat number of the HPRTB locus and structure of rare intermediate alleles
G Mertens, M Gielis, N Mommers, et al.
Journal of the Peripheral Nervous System : JPNS
|
July 10, 2001
Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT 1A
Y Rajabally, A Vital, X Ferrer, et al.
Journal of Medical Genetics
|
December 10, 2002
Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies
N Vandenberghe, M Upadhyaya, A Gatignol, et al.
Biochimie
|
January 1, 1971
Recent progress in the sequence determination of bacteriophage MS2 RNA
W Fiers, R Contreras, R De Wachter, et al.
Neurogastroenterology and Motility
|
March 4, 2009
A dose-ranging, placebo-controlled, pilot trial of Acotiamide in patients with functional dyspepsia
J Tack, A Masclee, R Heading, et al.
Genomics
|
May 1, 1990
The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF island
P Stinissen, W Van Hul, G Van Camp, et al.
Clinical Genetics
|
November 1, 1994
New allele of probe D17S61 present in the Charcot-Marie-Tooth 1A duplication
M Bost, C Bonnebouche, P M Gonnaud, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 126) with videos related to
Sort By:
Page
of 13
Clinical Genetics
|
January 5, 2001
Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients
N Bissar-Tadmouri, Y Parman, L Boutrand, et al.
Revue Neurologique
|
December 17, 2004
[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy]
B Degos, A Echaniz-Laguna, P Latour, et al.
Human Mutation
|
October 26, 1999
Two novel mutations in the MPZ gene coding region in Charcot-Marie-Tooth type 1 patients of Turkish origin: S54P, [I30del; GVYI29ins]
N Bissar-Tadmouri, Y Gulsen-Parman, P Latour, et al.
International Journal of Legal Medicine
|
May 21, 1999
Mutation of the repeat number of the HPRTB locus and structure of rare intermediate alleles
G Mertens, M Gielis, N Mommers, et al.
Journal of the Peripheral Nervous System : JPNS
|
July 10, 2001
Chronic inflammatory demyelinating polyneuropathy caused by HIV infection in a patient with asymptomatic CMT 1A
Y Rajabally, A Vital, X Ferrer, et al.
Journal of Medical Genetics
|
December 10, 2002
Frequency of mutations in the early growth response 2 gene associated with peripheral demyelinating neuropathies
N Vandenberghe, M Upadhyaya, A Gatignol, et al.
Biochimie
|
January 1, 1971
Recent progress in the sequence determination of bacteriophage MS2 RNA
W Fiers, R Contreras, R De Wachter, et al.
Neurogastroenterology and Motility
|
March 4, 2009
A dose-ranging, placebo-controlled, pilot trial of Acotiamide in patients with functional dyspepsia
J Tack, A Masclee, R Heading, et al.
Genomics
|
May 1, 1990
The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF island
P Stinissen, W Van Hul, G Van Camp, et al.
Clinical Genetics
|
November 1, 1994
New allele of probe D17S61 present in the Charcot-Marie-Tooth 1A duplication
M Bost, C Bonnebouche, P M Gonnaud, et al.
Page
of 13