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Nature
|
October 10, 1991
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
B Franco, S Guioli, A Pragliola, et al.
Nature Genetics
|
November 14, 1997
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
N A Quaderi, S Schweiger, K Gaudenz, et al.
American Journal of Medical Genetics
|
November 20, 1995
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome
A Renieri, L Galli, A Grillo, et al.
Human Molecular Genetics
|
April 18, 1998
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region
L Dal Zotto, N A Quaderi, R Elliott, et al.
American Journal of Human Genetics
|
January 13, 2000
Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance
M P Sperandeo, M T Bassi, M Riboni, et al.
American Journal of Human Genetics
|
June 1, 1996
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene
A Renieri, M Bruttini, L Galli, et al.
Human Molecular Genetics
|
February 7, 2001
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria
M A Font, L Feliubadaló, X Estivill, et al.
Oncogene
|
November 1, 2001
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas-a possible mechanism for altering the nm23-H1 activity
A Forus, A D'Angelo, J Henriksen, et al.
Scientific Reports
|
July 27, 2024
Cross-architecture tuning of silicon and SiGe-based quantum devices using machine learning
B Severin, D T Lennon, L C Camenzind, et al.
Nature Genetics
|
September 2, 1999
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT
L Feliubadaló, M Font, J Purroy, et al.
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of 20
Search research articles
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Showing results (191-200 of 200) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 200 results.
Nature
|
October 10, 1991
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
B Franco, S Guioli, A Pragliola, et al.
Nature Genetics
|
November 14, 1997
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
N A Quaderi, S Schweiger, K Gaudenz, et al.
American Journal of Medical Genetics
|
November 20, 1995
Major COL4A5 gene rearrangements in patients with juvenile type Alport syndrome
A Renieri, L Galli, A Grillo, et al.
Human Molecular Genetics
|
April 18, 1998
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region
L Dal Zotto, N A Quaderi, R Elliott, et al.
American Journal of Human Genetics
|
January 13, 2000
Structure of the SLC7A7 gene and mutational analysis of patients affected by lysinuric protein intolerance
M P Sperandeo, M T Bassi, M Riboni, et al.
American Journal of Human Genetics
|
June 1, 1996
X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene
A Renieri, M Bruttini, L Galli, et al.
Human Molecular Genetics
|
February 7, 2001
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuria
M A Font, L Feliubadaló, X Estivill, et al.
Oncogene
|
November 1, 2001
Amplification and overexpression of PRUNE in human sarcomas and breast carcinomas-a possible mechanism for altering the nm23-H1 activity
A Forus, A D'Angelo, J Henriksen, et al.
Scientific Reports
|
July 27, 2024
Cross-architecture tuning of silicon and SiGe-based quantum devices using machine learning
B Severin, D T Lennon, L C Camenzind, et al.
Nature Genetics
|
September 2, 1999
Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT
L Feliubadaló, M Font, J Purroy, et al.
Page
of 20