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Human Molecular Genetics
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February 28, 1998
Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene
G M Brown, R A Furlong, C A Sargent, et al.
Neuroradiology
|
May 8, 2024
(What's the story) morning glory? MRI findings in morning glory disc anomaly
Caoilfhionn Ní Leidhin, Jonathan P Erickson, Michael Bynevelt, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2008
The clinical spectrum of homozygous HOXA1 mutations
Thomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 9, 2000
Altered HOX and WNT7A expression in human lung cancer
R Calvo, J West, W Franklin, et al.
Genomics
|
December 1, 1987
Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17
S R Diehl, M Boehnke, R P Erickson, et al.
Behavioral and Brain Functions : BBF
|
July 11, 2006
Number of risk genotypes is a risk factor for major depressive disorder: a case control study
Holly A Garriock, Pedro Delgado, Mitchel A Kling, et al.
Mitochondrion
|
November 29, 2011
Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy
Maik Hüttemann, Scott Klewer, Icksoo Lee, et al.
American Journal of Human Genetics
|
January 1, 1989
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene
S R Diehl, M Boehnke, R P Erickson, et al.
The American Journal of Medicine
|
October 17, 2021
Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration Family
Debbie J Mustacich, Li-Wen Lai, Michael J Bernas, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 8, 2015
FtsZ filament capping by MciZ, a developmental regulator of bacterial division
Alexandre W Bisson-Filho, Karen F Discola, Patrícia Castellen, et al.
Page
of 70
Search research articles
Search
Showing results (671-680 of 698) with videos related to
Sort By:
Page
of 70
Human Molecular Genetics
|
February 28, 1998
Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene
G M Brown, R A Furlong, C A Sargent, et al.
Neuroradiology
|
May 8, 2024
(What's the story) morning glory? MRI findings in morning glory disc anomaly
Caoilfhionn Ní Leidhin, Jonathan P Erickson, Michael Bynevelt, et al.
American Journal of Medical Genetics. Part A
|
April 17, 2008
The clinical spectrum of homozygous HOXA1 mutations
Thomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 9, 2000
Altered HOX and WNT7A expression in human lung cancer
R Calvo, J West, W Franklin, et al.
Genomics
|
December 1, 1987
Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17
S R Diehl, M Boehnke, R P Erickson, et al.
Behavioral and Brain Functions : BBF
|
July 11, 2006
Number of risk genotypes is a risk factor for major depressive disorder: a case control study
Holly A Garriock, Pedro Delgado, Mitchel A Kling, et al.
Mitochondrion
|
November 29, 2011
Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy
Maik Hüttemann, Scott Klewer, Icksoo Lee, et al.
American Journal of Human Genetics
|
January 1, 1989
A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene
S R Diehl, M Boehnke, R P Erickson, et al.
The American Journal of Medicine
|
October 17, 2021
Digenic Inheritance of a FOXC2 Mutation and Two PIEZO1 Mutations Underlies Congenital Lymphedema in a Multigeneration Family
Debbie J Mustacich, Li-Wen Lai, Michael J Bernas, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 8, 2015
FtsZ filament capping by MciZ, a developmental regulator of bacterial division
Alexandre W Bisson-Filho, Karen F Discola, Patrícia Castellen, et al.
Page
of 70