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J P Welch

Showing results (111-120 of 118) with videos related to

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American Journal of Human Genetics|July 1, 1997
Linkage of Niemann-Pick disease type D to the same region of human chromosome 18 as Niemann-Pick disease type CW L Greer, D C Riddell, D M Byers, et al.
Nature|May 15, 1975
Non-random occurrence of 7-14 translocations in human lymphocyte culturesJ P Welch, C L Lee, J W Beatty-DeSana, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
The relationship between steroidogenic factor 1 and DAX-1 expression and in vitro gonadotropin secretion in human pituitary adenomasS J Aylwin, J P Welch, C L Davey, et al.
The Journal of Pediatrics|February 1, 1986
Further delineation of Weaver syndromeH H Ardinger, J W Hanson, M J Harrod, et al.
Clinical Biochemistry|February 10, 1998
Detection of a R173W mutation in the porphobilinogen deaminase gene in the Nova Scotian "foreign Protestant" population with acute intermittent porphyria: a founder effectS T Greene-Davis, P E Neumann, O E Mann, et al.
American Journal of Human Genetics|October 1, 1992
A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screeningB L Triggs-Raine, E H Mules, M M Kaback, et al.
Prenatal Diagnosis|July 27, 1999
Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT)E J Winsor, D J Tomkins, D Kalousek, et al.
Clinical Genetics|June 6, 2003
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000S Creighton, E W Almqvist, D MacGregor, et al.
Pageof 12

Showing results (111-120 of 118) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 118 results.
American Journal of Human Genetics|July 1, 1997
Linkage of Niemann-Pick disease type D to the same region of human chromosome 18 as Niemann-Pick disease type CW L Greer, D C Riddell, D M Byers, et al.
Nature|May 15, 1975
Non-random occurrence of 7-14 translocations in human lymphocyte culturesJ P Welch, C L Lee, J W Beatty-DeSana, et al.
The Journal of Clinical Endocrinology and Metabolism|June 9, 2001
The relationship between steroidogenic factor 1 and DAX-1 expression and in vitro gonadotropin secretion in human pituitary adenomasS J Aylwin, J P Welch, C L Davey, et al.
The Journal of Pediatrics|February 1, 1986
Further delineation of Weaver syndromeH H Ardinger, J W Hanson, M J Harrod, et al.
Clinical Biochemistry|February 10, 1998
Detection of a R173W mutation in the porphobilinogen deaminase gene in the Nova Scotian "foreign Protestant" population with acute intermittent porphyria: a founder effectS T Greene-Davis, P E Neumann, O E Mann, et al.
American Journal of Human Genetics|October 1, 1992
A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screeningB L Triggs-Raine, E H Mules, M M Kaback, et al.
Prenatal Diagnosis|July 27, 1999
Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT)E J Winsor, D J Tomkins, D Kalousek, et al.
Clinical Genetics|June 6, 2003
Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000S Creighton, E W Almqvist, D MacGregor, et al.
Pageof 12