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Donald W Hadley

Showing results (31-40 of 50) with videos related to

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JAMA|September 28, 2006
Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic reviewNoralane M Lindor, Gloria M Petersen, Donald W Hadley, et al.
BMC Cancer|April 2, 2020
The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: a case reportJohn G Aversa, Francine Blumental De Abreu, Sho Yano, et al.
American Journal of Medical Genetics. Part A|May 31, 2012
Patients within the Broad Holoprosencephaly Spectrum have Distinct and Subtle Ophthalmologic Anomalies: Response to KhanDaniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 18, 2013
Analysis of cardiac anomalies in VACTERL associationBridget K Cunningham, Donald W Hadley, Hwaida Hannoush, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 19, 2008
Perceptions of cancer risks and predictors of colon and endometrial cancer screening in women undergoing genetic testing for Lynch syndromeDonald W Hadley, Jean F Jenkins, Seth M Steinberg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2010
Generation after generation: exploring the psychological impact of providing genetic services through a cascading approachDonald W Hadley, Sato Ashida, Jean F Jenkins, et al.
American Journal of Medical Genetics. Part A|October 7, 2011
A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrumDaniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 25, 2011
De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate geneBenjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, et al.
Congenital Anomalies|July 4, 2017
SIX3 deletions and incomplete penetrance in families affected by holoprosencephalyBethany Stokes, Seth I Berger, Beth A Hall, et al.
American Journal of Medical Genetics. Part A|March 10, 2020
A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung diseaseElizabeth A Burke, Kyle E Reichard, Lynne A Wolfe, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
JAMA|September 28, 2006
Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic reviewNoralane M Lindor, Gloria M Petersen, Donald W Hadley, et al.
BMC Cancer|April 2, 2020
The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: a case reportJohn G Aversa, Francine Blumental De Abreu, Sho Yano, et al.
American Journal of Medical Genetics. Part A|May 31, 2012
Patients within the Broad Holoprosencephaly Spectrum have Distinct and Subtle Ophthalmologic Anomalies: Response to KhanDaniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|December 18, 2013
Analysis of cardiac anomalies in VACTERL associationBridget K Cunningham, Donald W Hadley, Hwaida Hannoush, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 19, 2008
Perceptions of cancer risks and predictors of colon and endometrial cancer screening in women undergoing genetic testing for Lynch syndromeDonald W Hadley, Jean F Jenkins, Seth M Steinberg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2010
Generation after generation: exploring the psychological impact of providing genetic services through a cascading approachDonald W Hadley, Sato Ashida, Jean F Jenkins, et al.
American Journal of Medical Genetics. Part A|October 7, 2011
A broad range of ophthalmologic anomalies is part of the holoprosencephaly spectrumDaniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 25, 2011
De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate geneBenjamin D Solomon, Daniel E Pineda-Alvarez, Donald W Hadley, et al.
Congenital Anomalies|July 4, 2017
SIX3 deletions and incomplete penetrance in families affected by holoprosencephalyBethany Stokes, Seth I Berger, Beth A Hall, et al.
American Journal of Medical Genetics. Part A|March 10, 2020
A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung diseaseElizabeth A Burke, Kyle E Reichard, Lynne A Wolfe, et al.
Pageof 5