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American Journal of Human Genetics
|
October 1, 1990
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232
T Meitinger, B Heye, C Petit, et al.
Nucleic Acids Research
|
October 11, 1991
A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3)
P M Bouloux, J P Hardelin, P Munroe, et al.
Cell
|
October 18, 1991
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
R Legouis, J P Hardelin, J Levilliers, et al.
Human Molecular Genetics
|
October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene
C Vincent, V Kalatzis, S Compain, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1992
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene
J P Hardelin, J Levilliers, I del Castillo, et al.
Genomics
|
June 1, 1993
Construction of a yeast artificial chromosome contig spanning the pseudoautosomal region and isolation of 25 new sequence-tagged sites
R Slim, D Le Paslier, S Compain, et al.
Journal of Cell Science
|
July 1, 1996
Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system
N Soussi-Yanicostas, J P Hardelin, M M Arroyo-Jimenez, et al.
Genomics
|
March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)
I Wang, B Franco, G B Ferrero, et al.
Cell
|
April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
B Franco, G Meroni, G Parenti, et al.
Human Molecular Genetics
|
October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene
F Denoyelle, D Weil, M A Maw, et al.
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of 5
Search research articles
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Showing results (41-50 of 50) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 50 results.
American Journal of Human Genetics
|
October 1, 1990
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232
T Meitinger, B Heye, C Petit, et al.
Nucleic Acids Research
|
October 11, 1991
A dinucleotide repeat polymorphism at the Kallmann locus (Xp22.3)
P M Bouloux, J P Hardelin, P Munroe, et al.
Cell
|
October 18, 1991
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
R Legouis, J P Hardelin, J Levilliers, et al.
Human Molecular Genetics
|
October 1, 1994
A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene
C Vincent, V Kalatzis, S Compain, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 1, 1992
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene
J P Hardelin, J Levilliers, I del Castillo, et al.
Genomics
|
June 1, 1993
Construction of a yeast artificial chromosome contig spanning the pseudoautosomal region and isolation of 25 new sequence-tagged sites
R Slim, D Le Paslier, S Compain, et al.
Journal of Cell Science
|
July 1, 1996
Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system
N Soussi-Yanicostas, J P Hardelin, M M Arroyo-Jimenez, et al.
Genomics
|
March 20, 1995
High-density physical mapping of a 3-Mb region in Xp22.3 and refined localization of the gene for X-linked recessive chondrodysplasia punctata (CDPX1)
I Wang, B Franco, G B Ferrero, et al.
Cell
|
April 7, 1995
A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy
B Franco, G Meroni, G Parenti, et al.
Human Molecular Genetics
|
October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene
F Denoyelle, D Weil, M A Maw, et al.
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of 5