F Hecht|B K Hecht - JoVE Visualize

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Cancer Genetics and Cytogenetics|January 15, 1986

Chromosome change in transitional cell carcinoma of ureterA A Sandberg, C S Berger, F S Haddad, et al.

Journal De Chirurgie|November 1, 1990

[Therapeutic diagram in advanced cancers of the esophagus]G Benhamou, J P Marmuse, H Johanet, et al.

Humangenetik|January 1, 1975

Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototypeR E Magenis, K Overton, H Wyandt, et al.

Human Genetics|March 12, 1976

9p trisomy identified by Giemsa-11H E Wyandt, F Hecht, R E Magenis, et al.

Obstetrics and Gynecology|March 1, 1984

Prenatal diagnosis of fragile (X) syndromeW A Hogge, S A Schonberg, T W Glover, et al.

Blood|June 1, 1978

Clonal evolution in atypical chronic granulocytic leukemia: a non-Philadelphia translocationG C Bagby, B Kaiser-McCaw, F Hecht, et al.

Genomics|February 1, 1990

Chromosome localization of human ARH genes, a ras-related gene familyL A Cannizzaro, P Madaule, F Hecht, et al.

Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|April 6, 2002

A confirmatory factor analysis of the WISC-III in a clinical sample with cross-validation in the standardization sampleD B Burton, A Sepehri, F Hecht, et al.

Biomedical Optics Express|July 5, 2021

Complex wavelet filter improves FLIM phasors for photon starved imaging experimentsP Wang, F Hecht, G Ossato, et al.

Cancer Genetics and Cytogenetics|November 1, 1981

Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemiaF P Li, F Hecht, B Kaiser-McCaw, et al.

Pageof 14

Showing results (111-120 of 138) with videos related to

Sort By:

Pageof 14

Cancer Genetics and Cytogenetics|January 15, 1986

Chromosome change in transitional cell carcinoma of ureterA A Sandberg, C S Berger, F S Haddad, et al.

Journal De Chirurgie|November 1, 1990

[Therapeutic diagram in advanced cancers of the esophagus]G Benhamou, J P Marmuse, H Johanet, et al.

Humangenetik|January 1, 1975

Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototypeR E Magenis, K Overton, H Wyandt, et al.

Human Genetics|March 12, 1976

9p trisomy identified by Giemsa-11H E Wyandt, F Hecht, R E Magenis, et al.

Obstetrics and Gynecology|March 1, 1984

Prenatal diagnosis of fragile (X) syndromeW A Hogge, S A Schonberg, T W Glover, et al.

Blood|June 1, 1978

Clonal evolution in atypical chronic granulocytic leukemia: a non-Philadelphia translocationG C Bagby, B Kaiser-McCaw, F Hecht, et al.

Genomics|February 1, 1990

Chromosome localization of human ARH genes, a ras-related gene familyL A Cannizzaro, P Madaule, F Hecht, et al.

Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|April 6, 2002

A confirmatory factor analysis of the WISC-III in a clinical sample with cross-validation in the standardization sampleD B Burton, A Sepehri, F Hecht, et al.

Biomedical Optics Express|July 5, 2021

Complex wavelet filter improves FLIM phasors for photon starved imaging experimentsP Wang, F Hecht, G Ossato, et al.

Cancer Genetics and Cytogenetics|November 1, 1981

Ataxia-pancytopenia: syndrome of cerebellar ataxia, hypoplastic anemia, monosomy 7, and acute myelogenous leukemiaF P Li, F Hecht, B Kaiser-McCaw, et al.

Pageof 14