Showing results (391-400 of 9,275) with videos related to

Sort By:
Pageof 928
American Journal of Medical Genetics. Part A|September 25, 2020
Caput membranaceum: A novel clinical presentation of ZIC1 related skull malformation and craniosynostosisErina Sasaki, Angela T Byrne, Dylan J Murray, et al.
American Journal of Medical Genetics. Part A|September 10, 2020
Use of complementary therapies for chronic pain management in patients with reported Ehlers-Danlos syndrome or hypermobility spectrum disordersJessica S Demes, Bryan McNair, Matthew R G Taylor
American Journal of Medical Genetics. Part A|September 11, 2020
Wolf-Hirschhorn syndrome: A case series from IndiaChakshu Chaudhry, Anit Kaur, Inusha Panigrahi, et al.
American Journal of Medical Genetics. Part A|September 29, 2020
Phenotypic diversity and genetic complexity of PAX3-related Waardenburg syndromePuneeth H Somashekar, Priyanka Upadhyai, Dhanya L Narayanan, et al.
American Journal of Medical Genetics. Part A|October 15, 2020
Epilepsy and movement disorders in CDG: Report on the oldest-known MOGS-CDG patientTommaso Lo Barco, Elisa Osanni, Andrea Bordugo, et al.
American Journal of Medical Genetics. Part A|January 7, 2020
Pathogenic variants in the TRIP11 gene cause a skeletal dysplasia spectrum from odontochondrodysplasia to achondrogenesis 1ACristina T N Medina, Renata Sandoval, Gabriela Oliveira, et al.
American Journal of Medical Genetics. Part A|March 21, 2020
Mowat-Wilson syndrome in a Chinese population: A case seriesStephanie Ho, Ho-Ming Luk, Brian Hon-Yin Chung, et al.
American Journal of Medical Genetics. Part A|March 21, 2020
Clinical, molecular, and pathological findings in a Neu-Laxova syndrome stillborn: A Brazilian case reportThiago R Cavole, Eduardo Perrone, Felipe S C Lucena de Castro, et al.
American Journal of Medical Genetics. Part A|March 13, 2020
Martsolf syndrome with novel mutation in the TBC1D20 gene in a family from IranHossein Hozhabri, Mehrdad Talebi, Mohammad Y V Mehrjardi, et al.
American Journal of Medical Genetics. Part A|February 1, 2020
Genetic evaluation including exome sequencing of two patients with Gomez-Lopez-Hernandez syndrome: Case reports and review of the literatureFaith Lindsay, Ilse Anderson, Ingrid M Wentzensen, et al.
Pageof 928