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European Journal of Human Genetics : EJHG
|
January 1, 1993
Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets
A Bolino, M Devoto, G Enia, et al.
American Journal of Human Genetics
|
May 1, 1995
Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus
K Nikali, A Suomalainen, J Terwilliger, et al.
Human Molecular Genetics
|
May 1, 1995
A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q
P Vincent, H Plauchu, J Hazan, et al.
Genomics
|
May 20, 1995
Physical mapping of 30 CA repeats on human chromosome 22
S Demczuk, O Delattre, A Vignal, et al.
Human Genetics
|
July 1, 1990
An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature
C Petit, J Melki, J Levilliers, et al.
American Journal of Medical Genetics
|
February 2, 1996
Refined genetic mapping of X-linked thoracoabdominal syndrome
R Parvari, R Carmi, J Weissenbach, et al.
The EMBO Journal
|
January 1, 1983
The beta2-microglobulin mRNA in human Daudi cells has a mutated initiation codon but is still inducible by interferon
F Rosa, H Berissi, J Weissenbach, et al.
Nature Genetics
|
July 1, 1994
Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness
D Weil, I Wang, A Dietrich, et al.
Genomics
|
May 15, 1996
YAC/STS map of 9 Mb of Xq26 at 100-kb resolution, localizing 6 ESTs, 6 genes, and 32 genetic markers
G Pilia, S MacMillan, R Nagaraja, et al.
Genome Research
|
July 1, 1997
Identification and chromosomal localization of human genes containing CAG/CTG repeats expressed in testis and brain
F Bulle, N Chiannilkulchai, A Pawlak, et al.
Page
of 37
Search research articles
Search
Showing results (71-80 of 363) with videos related to
Sort By:
Page
of 37
European Journal of Human Genetics : EJHG
|
January 1, 1993
Genetic mapping in the Xp11.2 region of a new form of X-linked hypophosphatemic rickets
A Bolino, M Devoto, G Enia, et al.
American Journal of Human Genetics
|
May 1, 1995
Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus
K Nikali, A Suomalainen, J Terwilliger, et al.
Human Molecular Genetics
|
May 1, 1995
A third locus for hereditary haemorrhagic telangiectasia maps to chromosome 12q
P Vincent, H Plauchu, J Hazan, et al.
Genomics
|
May 20, 1995
Physical mapping of 30 CA repeats on human chromosome 22
S Demczuk, O Delattre, A Vignal, et al.
Human Genetics
|
July 1, 1990
An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature
C Petit, J Melki, J Levilliers, et al.
American Journal of Medical Genetics
|
February 2, 1996
Refined genetic mapping of X-linked thoracoabdominal syndrome
R Parvari, R Carmi, J Weissenbach, et al.
The EMBO Journal
|
January 1, 1983
The beta2-microglobulin mRNA in human Daudi cells has a mutated initiation codon but is still inducible by interferon
F Rosa, H Berissi, J Weissenbach, et al.
Nature Genetics
|
July 1, 1994
Highly homologous loci on the X and Y chromosomes are hot-spots for ectopic recombinations leading to XX maleness
D Weil, I Wang, A Dietrich, et al.
Genomics
|
May 15, 1996
YAC/STS map of 9 Mb of Xq26 at 100-kb resolution, localizing 6 ESTs, 6 genes, and 32 genetic markers
G Pilia, S MacMillan, R Nagaraja, et al.
Genome Research
|
July 1, 1997
Identification and chromosomal localization of human genes containing CAG/CTG repeats expressed in testis and brain
F Bulle, N Chiannilkulchai, A Pawlak, et al.
Page
of 37