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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
September 1, 2019
Collaborating to advance interdisciplinary care for individuals with arthrogryposis
Noémi Dahan-Oliel, Judith G Hall
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 19, 2019
Fetal arthrogryposis: Challenges and perspectives for prenatal detection and management
Isabel Filges, Sevgi Tercanli, Judith G Hall
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 5, 2019
Classification of arthrogryposis
Judith G Hall, Eva Kimber, Klaus Dieterich
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 15, 2019
Central nervous system involvement in arthrogryposis multiplex congenita: Overview of causes, diagnosis, and care
Klaus Dieterich, Eva Kimber, Judith G Hall
American Journal of Medical Genetics. Part A
|
September 15, 2005
A syndrome characterized by contractures and pterygia of upper body associated with umbilical hernia, short stature, and distinctive face in an Arabic family
Stavit A Shalev, Ronen Spiegel, Judith G Hall
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 3, 2019
A standardized autopsy protocol for arthrogryposis (multiple congenital contractures)
Kerby C Oberg, Shino Magaki, Judith G Hall
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 13, 2021
Northwest Indigenous Art and the Inspiring Spirits
Judith G Hall, Maile M Taualii, Wedlidi Speck
Lancet (London, England)
|
July 17, 2007
Achondroplasia
William A Horton, Judith G Hall, Jacqueline T Hecht
American Journal of Medical Genetics. Part A
|
January 25, 2014
Amyoplasia revisited
Judith G Hall, Kimberly A Aldinger, Kimi I Tanaka
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
December 16, 2010
Prevalence of multiple congenital contractures including arthrogryposis multiplex congenita in Alberta, Canada, and a strategy for classification and coding
R Brian Lowry, Barbara Sibbald, Tanya Bedard, et al.
Page
of 11
Search research articles
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Showing results (61-70 of 104) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
September 1, 2019
Collaborating to advance interdisciplinary care for individuals with arthrogryposis
Noémi Dahan-Oliel, Judith G Hall
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 19, 2019
Fetal arthrogryposis: Challenges and perspectives for prenatal detection and management
Isabel Filges, Sevgi Tercanli, Judith G Hall
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 5, 2019
Classification of arthrogryposis
Judith G Hall, Eva Kimber, Klaus Dieterich
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 15, 2019
Central nervous system involvement in arthrogryposis multiplex congenita: Overview of causes, diagnosis, and care
Klaus Dieterich, Eva Kimber, Judith G Hall
American Journal of Medical Genetics. Part A
|
September 15, 2005
A syndrome characterized by contractures and pterygia of upper body associated with umbilical hernia, short stature, and distinctive face in an Arabic family
Stavit A Shalev, Ronen Spiegel, Judith G Hall
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
August 3, 2019
A standardized autopsy protocol for arthrogryposis (multiple congenital contractures)
Kerby C Oberg, Shino Magaki, Judith G Hall
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 13, 2021
Northwest Indigenous Art and the Inspiring Spirits
Judith G Hall, Maile M Taualii, Wedlidi Speck
Lancet (London, England)
|
July 17, 2007
Achondroplasia
William A Horton, Judith G Hall, Jacqueline T Hecht
American Journal of Medical Genetics. Part A
|
January 25, 2014
Amyoplasia revisited
Judith G Hall, Kimberly A Aldinger, Kimi I Tanaka
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
December 16, 2010
Prevalence of multiple congenital contractures including arthrogryposis multiplex congenita in Alberta, Canada, and a strategy for classification and coding
R Brian Lowry, Barbara Sibbald, Tanya Bedard, et al.
Page
of 11