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Human Genetics
|
June 1, 1991
The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)]
L Hills, E Earle, M Wilson, et al.
Human Genetics
|
March 1, 1990
Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome
M Schmidt, A Certoma, D Du Sart, et al.
American Journal of Medical Genetics
|
February 1, 1991
X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: application of the probe M27 beta to evaluate X inactivation status
M Schmidt, D Du Sart, P Kalitsis, et al.
Blood
|
January 29, 2000
Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia
P B Sinclair, E P Nacheva, M Leversha, et al.
Human Molecular Genetics
|
February 1, 1993
Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue
C A Sargent, N A Affara, E Bentley, et al.
Human Molecular Genetics
|
June 1, 1994
Molecular genetic analysis of the 3p- syndrome
M E Phipps, F Latif, A Prowse, et al.
Nature Genetics
|
October 15, 1998
Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene
A J Coffey, R A Brooksbank, O Brandau, et al.
Nature
|
January 10, 2002
The DNA sequence and comparative analysis of human chromosome 20
P Deloukas, L H Matthews, J Ashurst, et al.
Nature
|
May 28, 2004
DNA sequence and analysis of human chromosome 9
S J Humphray, K Oliver, A R Hunt, et al.
Nature
|
October 24, 2003
The DNA sequence and analysis of human chromosome 6
A J Mungall, S A Palmer, S K Sims, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Human Genetics
|
June 1, 1991
The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)]
L Hills, E Earle, M Wilson, et al.
Human Genetics
|
March 1, 1990
Unusual X chromosome inactivation in a mentally retarded girl with an interstitial deletion Xq27: implications for the fragile X syndrome
M Schmidt, A Certoma, D Du Sart, et al.
American Journal of Medical Genetics
|
February 1, 1991
X chromosome inactivation in fibroblasts of mentally retarded female carriers of the fragile site Xq27.3: application of the probe M27 beta to evaluate X inactivation status
M Schmidt, D Du Sart, P Kalitsis, et al.
Blood
|
January 29, 2000
Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia
P B Sinclair, E P Nacheva, M Leversha, et al.
Human Molecular Genetics
|
February 1, 1993
Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue
C A Sargent, N A Affara, E Bentley, et al.
Human Molecular Genetics
|
June 1, 1994
Molecular genetic analysis of the 3p- syndrome
M E Phipps, F Latif, A Prowse, et al.
Nature Genetics
|
October 15, 1998
Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene
A J Coffey, R A Brooksbank, O Brandau, et al.
Nature
|
January 10, 2002
The DNA sequence and comparative analysis of human chromosome 20
P Deloukas, L H Matthews, J Ashurst, et al.
Nature
|
May 28, 2004
DNA sequence and analysis of human chromosome 9
S J Humphray, K Oliver, A R Hunt, et al.
Nature
|
October 24, 2003
The DNA sequence and analysis of human chromosome 6
A J Mungall, S A Palmer, S K Sims, et al.
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of 3