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Showing results (21-30 of 25) with videos related to

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American Journal of Human Genetics|October 3, 1998
A gene for Meckel syndrome maps to chromosome 11q13J Roume, E Genin, V Cormier-Daire, et al.
Journal of Medical Genetics|May 4, 2004
Embryonic expression of the human MID1 gene and its mutations in Opitz syndromeL Pinson, J Augé, S Audollent, et al.
European Journal of Medical Genetics|November 5, 2018
Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcomeB Deloison, P Sonigo, A E Millischer-Bellaiche, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|May 21, 2024
Safety and efficacy of continuous terlipressin infusion in HRS-AKI in a transplant populationK Rajender Reddy, Ethan M Weinberg, Stevan A Gonzalez, et al.
Clinical Genetics|April 5, 2016
Refining the phenotypical and mutational spectrum of Taybi-Linder syndromeA Putoux, A Alqahtani, L Pinson, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
American Journal of Human Genetics|October 3, 1998
A gene for Meckel syndrome maps to chromosome 11q13J Roume, E Genin, V Cormier-Daire, et al.
Journal of Medical Genetics|May 4, 2004
Embryonic expression of the human MID1 gene and its mutations in Opitz syndromeL Pinson, J Augé, S Audollent, et al.
European Journal of Medical Genetics|November 5, 2018
Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcomeB Deloison, P Sonigo, A E Millischer-Bellaiche, et al.
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|May 21, 2024
Safety and efficacy of continuous terlipressin infusion in HRS-AKI in a transplant populationK Rajender Reddy, Ethan M Weinberg, Stevan A Gonzalez, et al.
Clinical Genetics|April 5, 2016
Refining the phenotypical and mutational spectrum of Taybi-Linder syndromeA Putoux, A Alqahtani, L Pinson, et al.
Pageof 3