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F Hecht

Showing results (151-160 of 350) with videos related to

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Cancer Genetics and Cytogenetics|February 1, 1986
T-cell cancer breakpoints at genes for T-cell receptor on chromosomes 7 and 14F Hecht, B K Hecht, R Morgan
Clinical Genetics|October 1, 1980
The use of sequential silver and quinacrine staining to determine the parental origin and breakpoints of a ring-22 human chromosomeG Fowler, B Kaiser-McCaw, F Hecht
The New England Journal of Medicine|November 8, 1973
Letter: Restrictive consent and amniocentesisF Hecht, P Garlinger, G H Prescott
Die Pharmazie|April 1, 1986
[Butaperazine blood level determination by radioimmunoassay following oral application of Tyrylen drug forms]I Hergert, H F Hecht, G Peinhardt
Cancer Genetics and Cytogenetics|October 1, 1988
Robertsonian chromosome recombinants are rare in cancerF Hecht, R Morgan, B K Hecht
International Archives of Allergy and Applied Immunology|January 1, 1970
Impaired in vitro response of circulating lymphocytes to phytohemagglutinin in Down's syndrome: dose- and time-response curves and relation to cellular immunityD A Rigas, P Elsasser, F Hecht
The New England Journal of Medicine|January 9, 1975
Parthenogenic origin of benign ovarian teratomasD Linder, B K McCaw, F Hecht
Clinical Genetics|January 1, 1989
"Unstable" translocation not proven unstableB K Hecht, D Lockwood, F Hecht
American Journal of Medical Genetics|August 1, 1989
Three additional cases of the congenital hypothalamic "hamartoblastoma" (Pallister-Hall) syndromeP D Pallister, F Hecht, J Herrman
American Journal of Medical Genetics|July 1, 1991
Forebrain cleavage gene causing holoprosencephaly: deletion mapping to chromosome band 2p21B K Hecht, F Hecht, M Münke
Pageof 35

Showing results (151-160 of 350) with videos related to

Sort By:
Pageof 35
Cancer Genetics and Cytogenetics|February 1, 1986
T-cell cancer breakpoints at genes for T-cell receptor on chromosomes 7 and 14F Hecht, B K Hecht, R Morgan
Clinical Genetics|October 1, 1980
The use of sequential silver and quinacrine staining to determine the parental origin and breakpoints of a ring-22 human chromosomeG Fowler, B Kaiser-McCaw, F Hecht
The New England Journal of Medicine|November 8, 1973
Letter: Restrictive consent and amniocentesisF Hecht, P Garlinger, G H Prescott
Die Pharmazie|April 1, 1986
[Butaperazine blood level determination by radioimmunoassay following oral application of Tyrylen drug forms]I Hergert, H F Hecht, G Peinhardt
Cancer Genetics and Cytogenetics|October 1, 1988
Robertsonian chromosome recombinants are rare in cancerF Hecht, R Morgan, B K Hecht
International Archives of Allergy and Applied Immunology|January 1, 1970
Impaired in vitro response of circulating lymphocytes to phytohemagglutinin in Down's syndrome: dose- and time-response curves and relation to cellular immunityD A Rigas, P Elsasser, F Hecht
The New England Journal of Medicine|January 9, 1975
Parthenogenic origin of benign ovarian teratomasD Linder, B K McCaw, F Hecht
Clinical Genetics|January 1, 1989
"Unstable" translocation not proven unstableB K Hecht, D Lockwood, F Hecht
American Journal of Medical Genetics|August 1, 1989
Three additional cases of the congenital hypothalamic "hamartoblastoma" (Pallister-Hall) syndromeP D Pallister, F Hecht, J Herrman
American Journal of Medical Genetics|July 1, 1991
Forebrain cleavage gene causing holoprosencephaly: deletion mapping to chromosome band 2p21B K Hecht, F Hecht, M Münke
Pageof 35