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The American Journal of Psychiatry
|
November 5, 2003
Familial and genetic effects on motor coordination, laterality, and reading-related cognition
Clyde Francks, Simon E Fisher, Angela J Marlow, et al.
Behavior Genetics
|
September 8, 2001
Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK
A J Marlow, S E Fisher, A J Richardson, et al.
Transplantation Proceedings
|
April 1, 1992
Use of xenogeneic islets in hybrid artificial pancreas for treatment of diabetes without immunosuppression
H Ohzato, M Carretta, T Maki, et al.
Human Molecular Genetics
|
June 17, 1999
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
E Maestrini, B P Korge, J Ocaña-Sierra, et al.
American Journal of Human Genetics
|
February 10, 2009
A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12
Julian E Asher, Janine A Lamb, Denise Brocklebank, et al.
Transplantation
|
July 1, 1987
The acquired immunodeficiency syndrome and transplantation
R H Rubin, R L Jenkins, B W Shaw, et al.
Cancer Immunology, Immunotherapy : CII
|
January 1, 1986
Non-human primate (baboon) anti-carcinoembryonic antigen antibody infusion in patients with metastatic adenocarcinoma. A phase I study
M S Huberman, J J Lokich, T Hill, et al.
Biological Psychiatry
|
April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
Tom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
Human Molecular Genetics
|
June 1, 1993
Fine mapping of the human SCIDX1 locus at Xq12-13.1
S Markiewicz, J P DiSanto, J Chelly, et al.
Clinical Nephrology
|
May 1, 1978
De novo development of membranous nephropathy in cadaver renal allografts
D R Steinmuller, M M Stilmant, B A Idelson, et al.
Page
of 72
Search research articles
Search
Showing results (561-570 of 719) with videos related to
Sort By:
Page
of 72
The American Journal of Psychiatry
|
November 5, 2003
Familial and genetic effects on motor coordination, laterality, and reading-related cognition
Clyde Francks, Simon E Fisher, Angela J Marlow, et al.
Behavior Genetics
|
September 8, 2001
Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK
A J Marlow, S E Fisher, A J Richardson, et al.
Transplantation Proceedings
|
April 1, 1992
Use of xenogeneic islets in hybrid artificial pancreas for treatment of diabetes without immunosuppression
H Ohzato, M Carretta, T Maki, et al.
Human Molecular Genetics
|
June 17, 1999
A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
E Maestrini, B P Korge, J Ocaña-Sierra, et al.
American Journal of Human Genetics
|
February 10, 2009
A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12
Julian E Asher, Janine A Lamb, Denise Brocklebank, et al.
Transplantation
|
July 1, 1987
The acquired immunodeficiency syndrome and transplantation
R H Rubin, R L Jenkins, B W Shaw, et al.
Cancer Immunology, Immunotherapy : CII
|
January 1, 1986
Non-human primate (baboon) anti-carcinoembryonic antigen antibody infusion in patients with metastatic adenocarcinoma. A phase I study
M S Huberman, J J Lokich, T Hill, et al.
Biological Psychiatry
|
April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
Tom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
Human Molecular Genetics
|
June 1, 1993
Fine mapping of the human SCIDX1 locus at Xq12-13.1
S Markiewicz, J P DiSanto, J Chelly, et al.
Clinical Nephrology
|
May 1, 1978
De novo development of membranous nephropathy in cadaver renal allografts
D R Steinmuller, M M Stilmant, B A Idelson, et al.
Page
of 72