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Neurology
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April 1, 2009
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H
G M Fabrizi, F Taioli, T Cavallaro, et al.
Genomics
|
December 28, 1999
A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes
G Kuhlenbäumer, A Schirmacher, J Meuleman, et al.
Antimicrobial Agents and Chemotherapy
|
October 23, 1997
Molecular biological characterization of an azole-resistant Candida glabrata isolate
P Marichal, H Vanden Bossche, F C Odds, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
December 6, 2016
Socioeconomic and modifiable predictors of blood pressure control for hypertension in primary care attenders in the Western Cape, South Africa
N Folb, M O Bachmann, E D Bateman, et al.
American Journal of Human Genetics
|
October 1, 1990
Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12
V Timmerman, P Raeymaekers, P De Jonghe, et al.
American Journal of Human Genetics
|
December 1, 1989
Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I)
P Raeymaekers, V Timmerman, P De Jonghe, et al.
Annals of the New York Academy of Sciences
|
December 10, 1999
A second family with autosomal dominant burning feet syndrome
G Kuhlenbäumer, P Young, R Kiefer, et al.
Journal of Virology
|
September 5, 2025
Intra-host SARS-CoV-2 diversity in immunocompromised people living with HIV provides insight into the evolutionary trajectory of SARS-CoV-2
R Joseph, G Marais, I Iranzadeh, et al.
Revue Neurologique
|
June 20, 2002
[Hereditary neuropathy with liability to pressure palsies: study of six Spanish families]
A Pou Serradell, J Monells, M J Téllez, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
A Second Family with Autosomal Dominant Burning Feet Syndrome
G Kuhlenbäumer, P Young, R Kiefer, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 105) with videos related to
Sort By:
Page
of 11
Neurology
|
April 1, 2009
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H
G M Fabrizi, F Taioli, T Cavallaro, et al.
Genomics
|
December 28, 1999
A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes
G Kuhlenbäumer, A Schirmacher, J Meuleman, et al.
Antimicrobial Agents and Chemotherapy
|
October 23, 1997
Molecular biological characterization of an azole-resistant Candida glabrata isolate
P Marichal, H Vanden Bossche, F C Odds, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
December 6, 2016
Socioeconomic and modifiable predictors of blood pressure control for hypertension in primary care attenders in the Western Cape, South Africa
N Folb, M O Bachmann, E D Bateman, et al.
American Journal of Human Genetics
|
October 1, 1990
Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12
V Timmerman, P Raeymaekers, P De Jonghe, et al.
American Journal of Human Genetics
|
December 1, 1989
Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I)
P Raeymaekers, V Timmerman, P De Jonghe, et al.
Annals of the New York Academy of Sciences
|
December 10, 1999
A second family with autosomal dominant burning feet syndrome
G Kuhlenbäumer, P Young, R Kiefer, et al.
Journal of Virology
|
September 5, 2025
Intra-host SARS-CoV-2 diversity in immunocompromised people living with HIV provides insight into the evolutionary trajectory of SARS-CoV-2
R Joseph, G Marais, I Iranzadeh, et al.
Revue Neurologique
|
June 20, 2002
[Hereditary neuropathy with liability to pressure palsies: study of six Spanish families]
A Pou Serradell, J Monells, M J Téllez, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
A Second Family with Autosomal Dominant Burning Feet Syndrome
G Kuhlenbäumer, P Young, R Kiefer, et al.
Page
of 11