Search research articles
Contact Us
Filters
Showing results (101-110 of 110) with videos related to
Page
of 11
Sort By:
You have reached the last page of results.
This site can display upto 110 results.
Clinical Genetics
|
October 23, 2014
Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome
D Oz-Levi, B Weiss, A Lahad, et al.
Current Topics in Developmental Biology
|
January 1, 1980
Complete primary structure of human histocompatibility antigen HLA-B7: evolutionary and functional implications
J L Strominger, V H Engelhard, B C Guild, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin
G Heimer, E Eyal, X Zhu, et al.
Clinical Genetics
|
April 5, 2016
A role for TENM1 mutations in congenital general anosmia
A Alkelai, T Olender, R Haffner-Krausz, et al.
Genomics
|
October 15, 1997
Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee
J A White, P J McAlpine, S Antonarakis, et al.
Gene
|
February 17, 2001
Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1
D Levanon, G Glusman, T Bangsow, et al.
Clinical Genetics
|
July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum
G Heimer, D Marek-Yagel, E Eyal, et al.
Nature Genetics
|
August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
I Eisenberg, N Avidan, T Potikha, et al.
Pharmacogenetics
|
August 1, 1997
The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence
P I Mackenzie, I S Owens, B Burchell, et al.
Nature
|
March 10, 2001
Initial sequencing and analysis of the human genome
E S Lander, L M Linton, B Birren, et al.
Page
of 11
Search research articles
Search
Showing results (101-110 of 110) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 110 results.
Clinical Genetics
|
October 23, 2014
Exome sequencing as a differential diagnosis tool: resolving mild trichohepatoenteric syndrome
D Oz-Levi, B Weiss, A Lahad, et al.
Current Topics in Developmental Biology
|
January 1, 1980
Complete primary structure of human histocompatibility antigen HLA-B7: evolutionary and functional implications
J L Strominger, V H Engelhard, B C Guild, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 3, 2017
Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin
G Heimer, E Eyal, X Zhu, et al.
Clinical Genetics
|
April 5, 2016
A role for TENM1 mutations in congenital general anosmia
A Alkelai, T Olender, R Haffner-Krausz, et al.
Genomics
|
October 15, 1997
Guidelines for human gene nomenclature (1997). HUGO Nomenclature Committee
J A White, P J McAlpine, S Antonarakis, et al.
Gene
|
February 17, 2001
Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1
D Levanon, G Glusman, T Bangsow, et al.
Clinical Genetics
|
July 4, 2015
SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum
G Heimer, D Marek-Yagel, E Eyal, et al.
Nature Genetics
|
August 31, 2001
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
I Eisenberg, N Avidan, T Potikha, et al.
Pharmacogenetics
|
August 1, 1997
The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence
P I Mackenzie, I S Owens, B Burchell, et al.
Nature
|
March 10, 2001
Initial sequencing and analysis of the human genome
E S Lander, L M Linton, B Birren, et al.
Page
of 11