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F Hecht

Showing results (251-260 of 350) with videos related to

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Clinical Genetics|February 1, 1986
Guidelines for the diagnosis of fragile XM A de Arce, F Hecht, G R Sutherland, et al.
Birth Defects Original Article Series|January 1, 1976
Human centromere mapping using teratoma dataJ Ott, F Hecht, D Linder, et al.
Blood|March 1, 1986
Cytogenetic and immunophenotypic analysis of cell lines established from patients with T cell leukemia/lymphomaS D Smith, R Morgan, M P Link, et al.
The American Journal of Medicine|June 1, 1984
Chromosome analysis in hematologic disorders. The leukemiasA A Sandberg, R Morgan, C Berger, et al.
Clinical Genetics|March 1, 1986
Genetic control over fragile X chromosome expressionF Hecht, J P Fryns, R F Vlietinck, et al.
Annals of Human Genetics|November 1, 1976
Estimating distances from the centromere by means of benign ovarian teratomas in manJ Ott, D Linder, B K McCaw, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|January 1, 2013
Early identification of young children with hearing loss in federally qualified health centersParul Bhatia, Sandra Mintz, Barbara F Hecht, et al.
Tissue Antigens|January 1, 1987
The human sex ratio: increase in first-born males to parents with shared HLA-DR antigensR M Radvany, N Vaisrub, C Ober, et al.
Annales De Genetique|December 1, 1972
Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome IIR E Magenis, S Armendares, F Hecht, et al.
Cancer Genetics and Cytogenetics|January 1, 1985
The Philadelphia (Ph) chromosome in leukemia. I. A new mechanism due to interstitial deletion and insertion in chronic myelocytic leukemiaF Hecht, R Morgan, S L Schrier, et al.
Pageof 35

Showing results (251-260 of 350) with videos related to

Sort By:
Pageof 35
Clinical Genetics|February 1, 1986
Guidelines for the diagnosis of fragile XM A de Arce, F Hecht, G R Sutherland, et al.
Birth Defects Original Article Series|January 1, 1976
Human centromere mapping using teratoma dataJ Ott, F Hecht, D Linder, et al.
Blood|March 1, 1986
Cytogenetic and immunophenotypic analysis of cell lines established from patients with T cell leukemia/lymphomaS D Smith, R Morgan, M P Link, et al.
The American Journal of Medicine|June 1, 1984
Chromosome analysis in hematologic disorders. The leukemiasA A Sandberg, R Morgan, C Berger, et al.
Clinical Genetics|March 1, 1986
Genetic control over fragile X chromosome expressionF Hecht, J P Fryns, R F Vlietinck, et al.
Annals of Human Genetics|November 1, 1976
Estimating distances from the centromere by means of benign ovarian teratomas in manJ Ott, D Linder, B K McCaw, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|January 1, 2013
Early identification of young children with hearing loss in federally qualified health centersParul Bhatia, Sandra Mintz, Barbara F Hecht, et al.
Tissue Antigens|January 1, 1987
The human sex ratio: increase in first-born males to parents with shared HLA-DR antigensR M Radvany, N Vaisrub, C Ober, et al.
Annales De Genetique|December 1, 1972
Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome IIR E Magenis, S Armendares, F Hecht, et al.
Cancer Genetics and Cytogenetics|January 1, 1985
The Philadelphia (Ph) chromosome in leukemia. I. A new mechanism due to interstitial deletion and insertion in chronic myelocytic leukemiaF Hecht, R Morgan, S L Schrier, et al.
Pageof 35