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F Hecht

Showing results (241-250 of 350) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|June 1, 1975
Somatic rearrangement of chromosome 14 in human lymphocytesB K McCaw, F Hecht, D G Harnden, et al.
Arizona Medicine|November 1, 1983
At increased risk: neural tube defect relativesF Hecht, B K Hecht, R C Wagner, et al.
Cytogenetics|January 1, 1971
Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+)H E Wyandt, F Hecht, E W Lovrien, et al.
Clinical Genetics|February 1, 1986
Population cytogenetics of autosomal fragile sitesP Petit, J P Fryns, H van den Berghe, et al.
Humangenetik|July 15, 1974
Colored reverse-banding of human chromosomes with acridine orange following alkaline-formalin treatment: densitometric validation and applicationsH E Wyandt, R F Vlietinck, R E Magenis, et al.
Cancer Genetics and Cytogenetics|March 15, 1986
The Philadelphia chromosome: a model of cancer and molecular cytogeneticsA A Sandberg, R M Gemmill, B K Hecht, et al.
Arizona Medicine|August 1, 1983
First-trimester prenatal diagnosis by trophoblast biopsyF Hecht, B K Hecht, H Bixenman, et al.
Arizona Medicine|October 1, 1982
Immunologic markers in the diagnosis of the acute lymphocytic leukemiasF Hecht, B K Hecht, T M Vyvial, et al.
Cancer Genetics and Cytogenetics|February 1, 1994
Nonrandom sex chromosome changes in brain tumorsF Hecht, B K Hecht, M Chatel, et al.
Blood|December 1, 1985
Leukemia with Down's syndrome: translocation between chromosomes 1 and 19 in acute myelomonocytic leukemia following transient congenital myeloproliferative syndromeR Morgan, F Hecht, M L Cleary, et al.
Pageof 35

Showing results (241-250 of 350) with videos related to

Sort By:
Pageof 35
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1975
Somatic rearrangement of chromosome 14 in human lymphocytesB K McCaw, F Hecht, D G Harnden, et al.
Arizona Medicine|November 1, 1983
At increased risk: neural tube defect relativesF Hecht, B K Hecht, R C Wagner, et al.
Cytogenetics|January 1, 1971
Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+)H E Wyandt, F Hecht, E W Lovrien, et al.
Clinical Genetics|February 1, 1986
Population cytogenetics of autosomal fragile sitesP Petit, J P Fryns, H van den Berghe, et al.
Humangenetik|July 15, 1974
Colored reverse-banding of human chromosomes with acridine orange following alkaline-formalin treatment: densitometric validation and applicationsH E Wyandt, R F Vlietinck, R E Magenis, et al.
Cancer Genetics and Cytogenetics|March 15, 1986
The Philadelphia chromosome: a model of cancer and molecular cytogeneticsA A Sandberg, R M Gemmill, B K Hecht, et al.
Arizona Medicine|August 1, 1983
First-trimester prenatal diagnosis by trophoblast biopsyF Hecht, B K Hecht, H Bixenman, et al.
Arizona Medicine|October 1, 1982
Immunologic markers in the diagnosis of the acute lymphocytic leukemiasF Hecht, B K Hecht, T M Vyvial, et al.
Cancer Genetics and Cytogenetics|February 1, 1994
Nonrandom sex chromosome changes in brain tumorsF Hecht, B K Hecht, M Chatel, et al.
Blood|December 1, 1985
Leukemia with Down's syndrome: translocation between chromosomes 1 and 19 in acute myelomonocytic leukemia following transient congenital myeloproliferative syndromeR Morgan, F Hecht, M L Cleary, et al.
Pageof 35