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Showing results (561-570 of 719) with videos related to

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The American Journal of Psychiatry|November 5, 2003
Familial and genetic effects on motor coordination, laterality, and reading-related cognitionClyde 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 UKA 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 immunosuppressionH 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 familiesE 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 12p12Julian E Asher, Janine A Lamb, Denise Brocklebank, et al.
Transplantation|July 1, 1987
The acquired immunodeficiency syndrome and transplantationR 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 studyM S Huberman, J J Lokich, T Hill, et al.
Biological Psychiatry|April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traitsTom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
Human Molecular Genetics|June 1, 1993
Fine mapping of the human SCIDX1 locus at Xq12-13.1S Markiewicz, J P DiSanto, J Chelly, et al.
Clinical Nephrology|May 1, 1978
De novo development of membranous nephropathy in cadaver renal allograftsD R Steinmuller, M M Stilmant, B A Idelson, et al.
Pageof 72

Showing results (561-570 of 719) with videos related to

Sort By:
Pageof 72
The American Journal of Psychiatry|November 5, 2003
Familial and genetic effects on motor coordination, laterality, and reading-related cognitionClyde 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 UKA 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 immunosuppressionH 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 familiesE 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 12p12Julian E Asher, Janine A Lamb, Denise Brocklebank, et al.
Transplantation|July 1, 1987
The acquired immunodeficiency syndrome and transplantationR 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 studyM S Huberman, J J Lokich, T Hill, et al.
Biological Psychiatry|April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traitsTom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
Human Molecular Genetics|June 1, 1993
Fine mapping of the human SCIDX1 locus at Xq12-13.1S Markiewicz, J P DiSanto, J Chelly, et al.
Clinical Nephrology|May 1, 1978
De novo development of membranous nephropathy in cadaver renal allograftsD R Steinmuller, M M Stilmant, B A Idelson, et al.
Pageof 72