About MWS - Mowat-Wilson Syndrome Foundation
Further Characterization of SMC1A Loss of Function Epilepsy Distinct From Cornelia de Lange Syndrome - Kristin W. Barañano, Amy Kimball, Susan L. Fong, Alena S. Egense, Catherine Hudon, Antonie D. Kline, 2022
Forgotten Diseases Research Foundation | Mowat-Wilson syndrome (MOWS)
About MWS - Mowat-Wilson Syndrome Foundation
A missense mutation in the ZFHX1B gene associated with an atypical Mowat–Wilson syndrome phenotype - Heinritz - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library
About MWS - Mowat-Wilson Syndrome Foundation
The Creation of MowatWilson.org | The University of Chicago Genetic Services
A Case Report of a Prenatally Missed Mowat-Wilson Syndrome With Isolated Corpus Callosum Agenesis - Nesrin Şenbil, Zeynep Arslan, Derya Beyza Sayın Kocakap, Yasemin Bilgili, 2021
About MWS - Mowat-Wilson Syndrome Foundation
Mowat-Wilson Syndrome - StoryMD
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care | Genetics in Medicine
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care | Genetics in Medicine
About MWS - Mowat-Wilson Syndrome Foundation
What is Mowat Wilson Syndrome? made incredibly EASY - YouTube
About MWS - Mowat-Wilson Syndrome Foundation
35. Mowat-Wilson Syndrome - Undergraduate Research
Angelman syndrome - Wikipedia
Mowat-Wilson syndrome | Journal of Medical Genetics
35. Mowat-Wilson Syndrome - Undergraduate Research
Mowat–Wilson syndrome - Wikipedia
Blogs | AmbitCare
Clinical characteristics of Polish patients with molecularly confirmed Mowat -Wilson syndrome | Journal of Applied Genetics
