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Nature Genetics
|
May 20, 1998
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome
S D Dreyer, G Zhou, A Baldini, et al.
Cancer Research
|
November 26, 1997
Loss of heterozygosity studies and deletion mapping identify two putative chromosome 14q tumor suppressor loci in renal oncocytomas
R F Schwerdtle, A Winterpacht, S Störkel, et al.
Human Molecular Genetics
|
December 23, 1999
Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression
D Prawitt, T Enklaar, G Klemm, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 15, 1992
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes
K Buiting, V Greger, B H Brownstein, et al.
American Journal of Medical Genetics
|
November 7, 1998
Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)
T Pihlajamaa, D J Prockop, J Faber, et al.
Cytogenetics and Cell Genetics
|
August 31, 2001
Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene ST5) and mouse chromosome 7
C Amid, A Bahr, A Mujica, et al.
Human Mutation
|
October 29, 1998
Ten novel mutations found in Aniridia
M T Wolf, B Lorenz, A Winterpacht, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 14, 1995
Systematic screening of an arrayed cDNA library by PCR
D J Munroe, R Loebbert, E Bric, et al.
Nature Genetics
|
May 1, 1994
Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations
N Bardeesy, D Falkoff, M J Petruzzi, et al.
Genes, Chromosomes & Cancer
|
March 1, 1991
Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare
B Royer-Pokora, S Ragg, B Heckl-Ostreicher, et al.
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Search research articles
Search
Showing results (81-90 of 120) with videos related to
Sort By:
Page
of 12
Nature Genetics
|
May 20, 1998
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome
S D Dreyer, G Zhou, A Baldini, et al.
Cancer Research
|
November 26, 1997
Loss of heterozygosity studies and deletion mapping identify two putative chromosome 14q tumor suppressor loci in renal oncocytomas
R F Schwerdtle, A Winterpacht, S Störkel, et al.
Human Molecular Genetics
|
December 23, 1999
Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression
D Prawitt, T Enklaar, G Klemm, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 15, 1992
A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes
K Buiting, V Greger, B H Brownstein, et al.
American Journal of Medical Genetics
|
November 7, 1998
Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)
T Pihlajamaa, D J Prockop, J Faber, et al.
Cytogenetics and Cell Genetics
|
August 31, 2001
Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene ST5) and mouse chromosome 7
C Amid, A Bahr, A Mujica, et al.
Human Mutation
|
October 29, 1998
Ten novel mutations found in Aniridia
M T Wolf, B Lorenz, A Winterpacht, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 14, 1995
Systematic screening of an arrayed cDNA library by PCR
D J Munroe, R Loebbert, E Bric, et al.
Nature Genetics
|
May 1, 1994
Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations
N Bardeesy, D Falkoff, M J Petruzzi, et al.
Genes, Chromosomes & Cancer
|
March 1, 1991
Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare
B Royer-Pokora, S Ragg, B Heckl-Ostreicher, et al.
Page
of 12