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A Micheil Innes

Showing results (1-10 of 156) with videos related to

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American Journal of Medical Genetics. Part A|July 30, 2025
45th Annual David Smith Workshop on Malformations and MorphogenesisAlison M Elliott, A Micheil Innes
American Journal of Medical Genetics. Part A|February 7, 2019
39th Annual David W. Smith Workshop on Malformations and Morphogenesis: Abstracts of the 2018 Annual MeetingKym M Boycott, A Micheil Innes
Clinical Dysmorphology|May 11, 2002
Bowen-Conradi syndrome in non Hutterite infantA Micheil Innes, R Brian Lowry
American Journal of Medical Genetics. Part A|May 5, 2021
Fifty years of recognizable patterns of human malformation: Insights and opportunitiesA Micheil Innes, Danielle C Lynch
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 22, 2023
Rod-cone dystrophy in an adult with GNB1-related disorder: An expansion of the phenotype and natural historyXiao-Ru Yang, Faazil Kassam, A Micheil Innes
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2018
Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further researchA Micheil Innes, Brenda L McInnes, David A Dyment
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2018
Unsolved recognizable patterns of human malformation: Challenges and opportunitiesKym M Boycott, David A Dyment, A Micheil Innes
SAGE Open Medical Case Reports|February 9, 2024
Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brotherRachel L Aubry, A Micheil Innes, Richard M Haber
Journal of Child Neurology|September 24, 2025
Epilepsy due to a <i>MED25</i> Homozygous Pathogenic Founder VariantAndy Cheuk-Him Ng, Sabrina D'Alfonso, A Micheil Innes, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 12, 2020
A diagnostic approach to syndromic retinal dystrophies with intellectual disabilityXiao-Ru Yang, Matthew D Benson, Ian M MacDonald, et al.
Pageof 16

Showing results (1-10 of 156) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics. Part A|July 30, 2025
45th Annual David Smith Workshop on Malformations and MorphogenesisAlison M Elliott, A Micheil Innes
American Journal of Medical Genetics. Part A|February 7, 2019
39th Annual David W. Smith Workshop on Malformations and Morphogenesis: Abstracts of the 2018 Annual MeetingKym M Boycott, A Micheil Innes
Clinical Dysmorphology|May 11, 2002
Bowen-Conradi syndrome in non Hutterite infantA Micheil Innes, R Brian Lowry
American Journal of Medical Genetics. Part A|May 5, 2021
Fifty years of recognizable patterns of human malformation: Insights and opportunitiesA Micheil Innes, Danielle C Lynch
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 22, 2023
Rod-cone dystrophy in an adult with GNB1-related disorder: An expansion of the phenotype and natural historyXiao-Ru Yang, Faazil Kassam, A Micheil Innes
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2018
Clinical and genetic heterogeneity in Dubowitz syndrome: Implications for diagnosis, management and further researchA Micheil Innes, Brenda L McInnes, David A Dyment
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|December 24, 2018
Unsolved recognizable patterns of human malformation: Challenges and opportunitiesKym M Boycott, David A Dyment, A Micheil Innes
SAGE Open Medical Case Reports|February 9, 2024
Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brotherRachel L Aubry, A Micheil Innes, Richard M Haber
Journal of Child Neurology|September 24, 2025
Epilepsy due to a <i>MED25</i> Homozygous Pathogenic Founder VariantAndy Cheuk-Him Ng, Sabrina D'Alfonso, A Micheil Innes, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 12, 2020
A diagnostic approach to syndromic retinal dystrophies with intellectual disabilityXiao-Ru Yang, Matthew D Benson, Ian M MacDonald, et al.
Pageof 16