A P MONACO - JoVE Visualize

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Human Molecular Genetics|November 1, 1994

Isolation of CA dinucleotide repeats close to D6S105; linkage disequilibrium with haemochromatosisC Stone, J J Pointon, E C Jazwinska, et al.

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 23, 1999

Current thinking on chronic renal allograft rejection: issues, concerns, and recommendations from a 1997 roundtable discussionA P Monaco, J F Burke, R M Ferguson, 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.

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.

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.

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.

Genomics|March 1, 1994

Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell linesF Francis, F Benham, C G See, et al.

Genomics|April 1, 1988

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy geneM Burmeister, A P Monaco, E F Gillard, et al.

Nature Genetics|June 1, 1992

Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate regionG P Bates, J Valdes, H Hummerich, et al.

Pageof 29

Showing results (211-220 of 285) with videos related to

Sort By:

Pageof 29

Human Molecular Genetics|November 1, 1994

Isolation of CA dinucleotide repeats close to D6S105; linkage disequilibrium with haemochromatosisC Stone, J J Pointon, E C Jazwinska, et al.

American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 23, 1999

Current thinking on chronic renal allograft rejection: issues, concerns, and recommendations from a 1997 roundtable discussionA P Monaco, J F Burke, R M Ferguson, 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.

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.

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.

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.

Genomics|March 1, 1994

Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell linesF Francis, F Benham, C G See, et al.

Genomics|April 1, 1988

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy geneM Burmeister, A P Monaco, E F Gillard, et al.

Nature Genetics|June 1, 1992

Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate regionG P Bates, J Valdes, H Hummerich, et al.

Pageof 29