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Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
September 4, 1999
Quality of life in low-income patients with metastatic prostate cancer: divergent and convergent validity of three instruments
L K Sharp, S J Knight, R Nadler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1990
Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage
S T Warren, S J Knight, J F Peters, et al.
European Urology
|
January 1, 1997
A comparison of perspectives on prostate cancer: analysis of utility assessments of patients and physicians
C L Bennett, G Chapman, A S Elstein, et al.
American Journal of Medical Genetics
|
March 17, 2001
Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13)
B B de Vries, M Lees, S J Knight, et al.
Human Molecular Genetics
|
December 1, 1994
The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter
R J Ritchie, S J Knight, M C Hirst, et al.
American Journal of Human Genetics
|
June 1, 1996
PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28
S Lindsay, M Splitt, S Edney, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1997
Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
S J Knight, S W Horsley, R Regan, et al.
Lancet (London, England)
|
November 24, 1999
Subtle chromosomal rearrangements in children with unexplained mental retardation
S J Knight, R Regan, A Nicod, et al.
Clinical Genetics
|
January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome
B B de Vries, M Bitner-Glindzicz, S J Knight, et al.
Journal of Medical Genetics
|
September 11, 1998
Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements
S W Horsley, S J Knight, J Nixon, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 51) with videos related to
Sort By:
Page
of 6
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
September 4, 1999
Quality of life in low-income patients with metastatic prostate cancer: divergent and convergent validity of three instruments
L K Sharp, S J Knight, R Nadler, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1990
Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage
S T Warren, S J Knight, J F Peters, et al.
European Urology
|
January 1, 1997
A comparison of perspectives on prostate cancer: analysis of utility assessments of patients and physicians
C L Bennett, G Chapman, A S Elstein, et al.
American Journal of Medical Genetics
|
March 17, 2001
Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13)
B B de Vries, M Lees, S J Knight, et al.
Human Molecular Genetics
|
December 1, 1994
The cloning of FRAXF: trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter
R J Ritchie, S J Knight, M C Hirst, et al.
American Journal of Human Genetics
|
June 1, 1996
PPM-X: a new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28
S Lindsay, M Splitt, S Edney, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1997
Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
S J Knight, S W Horsley, R Regan, et al.
Lancet (London, England)
|
November 24, 1999
Subtle chromosomal rearrangements in children with unexplained mental retardation
S J Knight, R Regan, A Nicod, et al.
Clinical Genetics
|
January 10, 2001
A boy with a submicroscopic 22qter deletion, general overgrowth and features suggestive of FG syndrome
B B de Vries, M Bitner-Glindzicz, S J Knight, et al.
Journal of Medical Genetics
|
September 11, 1998
Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements
S W Horsley, S J Knight, J Nixon, et al.
Page
of 6