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Brad T Tinkle

Showing results (11-20 of 24) with videos related to

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The Journal of Pediatrics|July 18, 2009
Sleep-related respiratory abnormalities and arousal pattern in achondroplasia during early infancyMathew Ednick, Brad T Tinkle, Jungrak Phromchairak, et al.
The Journal of Pediatrics|January 4, 2011
Cross-sectional and longitudinal assessment of aortic root dilation and valvular anomalies in hypermobile and classic Ehlers-Danlos syndromeCarrie L Atzinger, Richard A Meyer, Philip R Khoury, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
Long-term survival in a patient with del(18)(q12.2q21.1)Brad T Tinkle, Carol A Christianson, Elizabeth K Schorry, et al.
American Journal of Medical Genetics. Part A|October 21, 2009
The lack of clinical distinction between the hypermobility type of Ehlers-Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome)Brad T Tinkle, Howard A Bird, Rodney Grahame, et al.
American Journal of Medical Genetics. Part A|November 12, 2005
Epidemiology of hemimegalencephaly: a case series and reviewBrad T Tinkle, Elizabeth K Schorry, David N Franz, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
Unexpected survival in a case of prenatally diagnosed non-mosaic trisomy 22: Clinical report and review of the natural historyBrad T Tinkle, Martha E Walker, Ruthann I Blough-Pfau, et al.
Annals of Vascular Surgery|January 20, 2015
Spontaneous ruptured dissection of the right common iliac artery in a patient with classic Ehlers-Danlos syndrome phenotypeRick Gaines, Brad T Tinkle, Pegge M Halandras, et al.
Journal of Child Health Care : for Professionals Working with Children in the Hospital and Community|August 3, 2019
Symptom complaints and impact on functioning in youth with hypermobile Ehlers-Danlos syndromeSusan T Tran, Anjana Jagpal, Marissa L Koven, et al.
American Journal of Medical Genetics. Part A|February 22, 2011
Variable expression of neurofibromatosis 1 in monozygotic twinsMargaret B Rieley, David A Stevenson, David H Viskochil, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|March 26, 2013
Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing lossTheru A Sivakumaran, Ammar Husami, Diane Kissell, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
The Journal of Pediatrics|July 18, 2009
Sleep-related respiratory abnormalities and arousal pattern in achondroplasia during early infancyMathew Ednick, Brad T Tinkle, Jungrak Phromchairak, et al.
The Journal of Pediatrics|January 4, 2011
Cross-sectional and longitudinal assessment of aortic root dilation and valvular anomalies in hypermobile and classic Ehlers-Danlos syndromeCarrie L Atzinger, Richard A Meyer, Philip R Khoury, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
Long-term survival in a patient with del(18)(q12.2q21.1)Brad T Tinkle, Carol A Christianson, Elizabeth K Schorry, et al.
American Journal of Medical Genetics. Part A|October 21, 2009
The lack of clinical distinction between the hypermobility type of Ehlers-Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome)Brad T Tinkle, Howard A Bird, Rodney Grahame, et al.
American Journal of Medical Genetics. Part A|November 12, 2005
Epidemiology of hemimegalencephaly: a case series and reviewBrad T Tinkle, Elizabeth K Schorry, David N Franz, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
Unexpected survival in a case of prenatally diagnosed non-mosaic trisomy 22: Clinical report and review of the natural historyBrad T Tinkle, Martha E Walker, Ruthann I Blough-Pfau, et al.
Annals of Vascular Surgery|January 20, 2015
Spontaneous ruptured dissection of the right common iliac artery in a patient with classic Ehlers-Danlos syndrome phenotypeRick Gaines, Brad T Tinkle, Pegge M Halandras, et al.
Journal of Child Health Care : for Professionals Working with Children in the Hospital and Community|August 3, 2019
Symptom complaints and impact on functioning in youth with hypermobile Ehlers-Danlos syndromeSusan T Tran, Anjana Jagpal, Marissa L Koven, et al.
American Journal of Medical Genetics. Part A|February 22, 2011
Variable expression of neurofibromatosis 1 in monozygotic twinsMargaret B Rieley, David A Stevenson, David H Viskochil, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|March 26, 2013
Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing lossTheru A Sivakumaran, Ammar Husami, Diane Kissell, et al.
Pageof 3