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Roberta A Pagon

Showing results (11-20 of 21) with videos related to

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American Journal of Medical Genetics. Part A|September 19, 2009
Partial ATRX gene duplication causes ATR-X syndromeDianne M Cohn, Roberta A Pagon, Louanne Hudgins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2011
Implementation outcomes of a multiinstitutional web-based ethical, legal, and social implications genetics curriculum for primary care residents in three specialtiesMalathi Srinivasan, Frank C Day, Erin Griffin, et al.
The Journal of Molecular Diagnostics : JMD|August 2, 2008
Ordering molecular genetic tests and reporting results: practices in laboratory and clinical settingsIra M Lubin, Michele Caggana, Carolyn Constantin, et al.
American Journal of Medical Genetics. Part A|May 15, 2012
Ambiguous genitalia: what prenatal genetic testing is practical?Margaret P Adam, Patricia Y Fechner, Linda A Ramsdell, et al.
The Journal of Molecular Diagnostics : JMD|February 7, 2009
Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory reportIra M Lubin, Margaret M McGovern, Zoe Gibson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2007
A Gender Assessment Team: experience with 250 patients over a period of 25 yearsMelissa A Parisi, Linda A Ramsdell, Mark W Burns, et al.
Human Mutation|April 23, 2002
GeneTests-GeneClinics: genetic testing information for a growing audienceRoberta A Pagon, Peter Tarczy-Hornoch, Patricia K Baskin, et al.
American Journal of Epidemiology|June 6, 2009
Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseasesMuin J Khoury, Lars Bertram, Paolo Boffetta, et al.
American Journal of Human Genetics|March 2, 2005
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutationsJennifer J Johnston, Isabelle Olivos-Glander, Christina Killoran, et al.
American Journal of Human Genetics|September 3, 2021
Response to Hamosh et alLeslie G Biesecker, Margaret P Adam, Fowzan S Alkuraya, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|September 19, 2009
Partial ATRX gene duplication causes ATR-X syndromeDianne M Cohn, Roberta A Pagon, Louanne Hudgins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2011
Implementation outcomes of a multiinstitutional web-based ethical, legal, and social implications genetics curriculum for primary care residents in three specialtiesMalathi Srinivasan, Frank C Day, Erin Griffin, et al.
The Journal of Molecular Diagnostics : JMD|August 2, 2008
Ordering molecular genetic tests and reporting results: practices in laboratory and clinical settingsIra M Lubin, Michele Caggana, Carolyn Constantin, et al.
American Journal of Medical Genetics. Part A|May 15, 2012
Ambiguous genitalia: what prenatal genetic testing is practical?Margaret P Adam, Patricia Y Fechner, Linda A Ramsdell, et al.
The Journal of Molecular Diagnostics : JMD|February 7, 2009
Clinician perspectives about molecular genetic testing for heritable conditions and development of a clinician-friendly laboratory reportIra M Lubin, Margaret M McGovern, Zoe Gibson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 19, 2007
A Gender Assessment Team: experience with 250 patients over a period of 25 yearsMelissa A Parisi, Linda A Ramsdell, Mark W Burns, et al.
Human Mutation|April 23, 2002
GeneTests-GeneClinics: genetic testing information for a growing audienceRoberta A Pagon, Peter Tarczy-Hornoch, Patricia K Baskin, et al.
American Journal of Epidemiology|June 6, 2009
Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseasesMuin J Khoury, Lars Bertram, Paolo Boffetta, et al.
American Journal of Human Genetics|March 2, 2005
Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutationsJennifer J Johnston, Isabelle Olivos-Glander, Christina Killoran, et al.
American Journal of Human Genetics|September 3, 2021
Response to Hamosh et alLeslie G Biesecker, Margaret P Adam, Fowzan S Alkuraya, et al.
Pageof 3