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Brad Tinkle

Showing results (1-10 of 11) with videos related to

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Human Genetics|June 29, 2007
Gene symbol: FBN1Brad Tinkle
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 18, 2017
The international consortium on the Ehlers-Danlos syndromesLara Bloom, Peter Byers, Clair Francomano, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 2, 2017
A framework for the classification of joint hypermobility and related conditionsMarco Castori, Brad Tinkle, Howard Levy, et al.
American Journal of Medical Genetics. Part A|September 14, 2019
Response to letter, broken bones, and irresponsible testimony: Enough is enough already: The flawed Ehlers-Danlos syndrome infant fragility theory should not ruleNatasha Shur, Brad Tinkle, Marshall Summar, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 11, 2017
Pain management in the Ehlers-Danlos syndromesPradeep Chopra, Brad Tinkle, Claude Hamonet, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 2, 2017
Hypermobile Ehlers-Danlos syndrome (a.k.a. Ehlers-Danlos syndrome Type III and Ehlers-Danlos syndrome hypermobility type): Clinical description and natural historyBrad Tinkle, Marco Castori, Britta Berglund, et al.
American Journal of Medical Genetics. Part A|October 1, 2019
Invited commentary: His life was lost but his heart still beats: In honor of children harmed by child abuseNatasha Shur, Tanya Hinds, Eglal Shalaby-Rana, et al.
Prenatal Diagnosis|August 9, 2014
Predictive value of fetal lung volume in prenatally diagnosed skeletal dysplasiaK Nicole Weaver, Jodie Johnson, Beth Kline-Fath, et al.
The Journal of Pediatrics|July 22, 2017
Newborn Screening for Lysosomal Storage Disorders in Illinois: The Initial 15-Month ExperienceBarbara K Burton, Joel Charrow, George E Hoganson, et al.
Human Mutation|March 19, 2021
More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndromeTibbe Dhooge, Tim Van Damme, Delfien Syx, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Human Genetics|June 29, 2007
Gene symbol: FBN1Brad Tinkle
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 18, 2017
The international consortium on the Ehlers-Danlos syndromesLara Bloom, Peter Byers, Clair Francomano, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 2, 2017
A framework for the classification of joint hypermobility and related conditionsMarco Castori, Brad Tinkle, Howard Levy, et al.
American Journal of Medical Genetics. Part A|September 14, 2019
Response to letter, broken bones, and irresponsible testimony: Enough is enough already: The flawed Ehlers-Danlos syndrome infant fragility theory should not ruleNatasha Shur, Brad Tinkle, Marshall Summar, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 11, 2017
Pain management in the Ehlers-Danlos syndromesPradeep Chopra, Brad Tinkle, Claude Hamonet, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 2, 2017
Hypermobile Ehlers-Danlos syndrome (a.k.a. Ehlers-Danlos syndrome Type III and Ehlers-Danlos syndrome hypermobility type): Clinical description and natural historyBrad Tinkle, Marco Castori, Britta Berglund, et al.
American Journal of Medical Genetics. Part A|October 1, 2019
Invited commentary: His life was lost but his heart still beats: In honor of children harmed by child abuseNatasha Shur, Tanya Hinds, Eglal Shalaby-Rana, et al.
Prenatal Diagnosis|August 9, 2014
Predictive value of fetal lung volume in prenatally diagnosed skeletal dysplasiaK Nicole Weaver, Jodie Johnson, Beth Kline-Fath, et al.
The Journal of Pediatrics|July 22, 2017
Newborn Screening for Lysosomal Storage Disorders in Illinois: The Initial 15-Month ExperienceBarbara K Burton, Joel Charrow, George E Hoganson, et al.
Human Mutation|March 19, 2021
More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndromeTibbe Dhooge, Tim Van Damme, Delfien Syx, et al.
Pageof 2