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F Hecht

Showing results (261-270 of 350) with videos related to

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Neurofibromatosis|January 1, 1988
Hereditary intestinal neurofibromatosis. I. A distinctive genetic diseaseR Heimann, A Verhest, J Verschraegen, et al.
Cancer Genetics and Cytogenetics|September 1, 1982
Translocations involving chromosomes #3 and #12: hematologic diseases associated with abnormalities of these chromosomesA A Sandberg, B K Hecht, S M Ondreyco, et al.
American Journal of Medical Genetics|November 1, 1993
Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literatureH A Hales, C M Peterson, J Carey, et al.
Cancer Genetics and Cytogenetics|June 1, 1988
Inversion of chromosome 5 long arm in region of cell growth gene cluster in hematologic disordersR Morgan, T A Walter, H J Decker, et al.
Birth Defects Original Article Series|January 1, 1978
Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studiesS R Patil, B Kaiser-McCaw, F Hecht, et al.
Arizona Medicine|November 1, 1980
The fragile X chromosome mental retardation and large testesF Hecht, B Kaiser-McCaw, B C Moore, et al.
Stroke|February 1, 2014
Effect of a novel video game on stroke knowledge of 9- to 10-year-old, low-income childrenOlajide Williams, Mindy F Hecht, Alexandra L DeSorbo, et al.
Cancer Genetics and Cytogenetics|March 15, 1986
Chromosome clues to acute leukemia in Down's syndromeF Hecht, B K Hecht, R Morgan, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 1, 1986
13-cis retinoic acid treatment for myelodysplastic syndromesV J Picozzi, G F Swanson, R Morgan, et al.
Development and Psychopathology|July 23, 2014
Moderation of maltreatment effects on childhood borderline personality symptoms by gender and oxytocin receptor and FK506 binding protein 5 genesDante Cicchetti, Fred A Rogosch, Kathryn F Hecht, et al.
Pageof 35

Showing results (261-270 of 350) with videos related to

Sort By:
Pageof 35
Neurofibromatosis|January 1, 1988
Hereditary intestinal neurofibromatosis. I. A distinctive genetic diseaseR Heimann, A Verhest, J Verschraegen, et al.
Cancer Genetics and Cytogenetics|September 1, 1982
Translocations involving chromosomes #3 and #12: hematologic diseases associated with abnormalities of these chromosomesA A Sandberg, B K Hecht, S M Ondreyco, et al.
American Journal of Medical Genetics|November 1, 1993
Prenatal detection of de novo paracentric inversion 46, XX inv (14) (q22q32.1) in a normal child: report and review of the literatureH A Hales, C M Peterson, J Carey, et al.
Cancer Genetics and Cytogenetics|June 1, 1988
Inversion of chromosome 5 long arm in region of cell growth gene cluster in hematologic disordersR Morgan, T A Walter, H J Decker, et al.
Birth Defects Original Article Series|January 1, 1978
Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studiesS R Patil, B Kaiser-McCaw, F Hecht, et al.
Arizona Medicine|November 1, 1980
The fragile X chromosome mental retardation and large testesF Hecht, B Kaiser-McCaw, B C Moore, et al.
Stroke|February 1, 2014
Effect of a novel video game on stroke knowledge of 9- to 10-year-old, low-income childrenOlajide Williams, Mindy F Hecht, Alexandra L DeSorbo, et al.
Cancer Genetics and Cytogenetics|March 15, 1986
Chromosome clues to acute leukemia in Down's syndromeF Hecht, B K Hecht, R Morgan, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 1, 1986
13-cis retinoic acid treatment for myelodysplastic syndromesV J Picozzi, G F Swanson, R Morgan, et al.
Development and Psychopathology|July 23, 2014
Moderation of maltreatment effects on childhood borderline personality symptoms by gender and oxytocin receptor and FK506 binding protein 5 genesDante Cicchetti, Fred A Rogosch, Kathryn F Hecht, et al.
Pageof 35