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American Journal of Medical Genetics. Part A
|
October 15, 2013
Elements of morphology: general terms for congenital anomalies
Raoul C Hennekam, Leslie G Biesecker, Judith E Allanson, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
July 26, 2021
Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning
Jenny van Dongen, Scott D Gordon, Veronika V Odintsova, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
September 27, 2006
A meeting of minds: interdisciplinary research in the health sciences in Canada
Judith G Hall, Lesley Bainbridge, Alison Buchan, et al.
American Journal of Medical Genetics. Part A
|
December 9, 2022
Perspectives on the future of dysmorphology
Benjamin D Solomon, Margaret P Adam, Chin-To Fong, et al.
Developmental Medicine and Child Neurology
|
April 9, 2024
Éléments de données communs pour l'arthrogrypose multiple congénitale: Un cadre international
Shahrzad Nematollahi, Klaus Dieterich, Isabel Filges, et al.
Developmental Medicine and Child Neurology
|
April 6, 2024
Elementos de datos comunes para la artrogriposis múltiple congénita: Un marco internacional
Shahrzad Nematollahi, Klaus Dieterich, Isabel Filges, et al.
Developmental Medicine and Child Neurology
|
March 16, 2024
Common data elements for arthrogryposis multiplex congenita: An international framework
Shahrzad Nematollahi, Klaus Dieterich, Isabel Filges, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 9, 2019
International multidisciplinary collaboration toward an annotated definition of arthrogryposis multiplex congenita
Noémi Dahan-Oliel, Sarah Cachecho, Douglas Barnes, et al.
Molecular Genetics & Genomic Medicine
|
August 7, 2015
Novel pathogenic variants and genes for myopathies identified by whole exome sequencing
Jesse M Hunter, Mary Ellen Ahearn, Christopher D Balak, et al.
American Journal of Medical Genetics. Part A
|
November 18, 2020
The spectrum of brain malformations and disruptions in twins
Kaylee B Park, Teresa Chapman, Kimberly A Aldinger, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 104) with videos related to
Sort By:
Page
of 11
American Journal of Medical Genetics. Part A
|
October 15, 2013
Elements of morphology: general terms for congenital anomalies
Raoul C Hennekam, Leslie G Biesecker, Judith E Allanson, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
|
July 26, 2021
Examining the Vanishing Twin Hypothesis of Neural Tube Defects: Application of an Epigenetic Predictor for Monozygotic Twinning
Jenny van Dongen, Scott D Gordon, Veronika V Odintsova, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
September 27, 2006
A meeting of minds: interdisciplinary research in the health sciences in Canada
Judith G Hall, Lesley Bainbridge, Alison Buchan, et al.
American Journal of Medical Genetics. Part A
|
December 9, 2022
Perspectives on the future of dysmorphology
Benjamin D Solomon, Margaret P Adam, Chin-To Fong, et al.
Developmental Medicine and Child Neurology
|
April 9, 2024
Éléments de données communs pour l'arthrogrypose multiple congénitale: Un cadre international
Shahrzad Nematollahi, Klaus Dieterich, Isabel Filges, et al.
Developmental Medicine and Child Neurology
|
April 6, 2024
Elementos de datos comunes para la artrogriposis múltiple congénita: Un marco internacional
Shahrzad Nematollahi, Klaus Dieterich, Isabel Filges, et al.
Developmental Medicine and Child Neurology
|
March 16, 2024
Common data elements for arthrogryposis multiplex congenita: An international framework
Shahrzad Nematollahi, Klaus Dieterich, Isabel Filges, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
July 9, 2019
International multidisciplinary collaboration toward an annotated definition of arthrogryposis multiplex congenita
Noémi Dahan-Oliel, Sarah Cachecho, Douglas Barnes, et al.
Molecular Genetics & Genomic Medicine
|
August 7, 2015
Novel pathogenic variants and genes for myopathies identified by whole exome sequencing
Jesse M Hunter, Mary Ellen Ahearn, Christopher D Balak, et al.
American Journal of Medical Genetics. Part A
|
November 18, 2020
The spectrum of brain malformations and disruptions in twins
Kaylee B Park, Teresa Chapman, Kimberly A Aldinger, et al.
Page
of 11