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
Clinical and Mutational Spectrum of Mowat–Wilson Syndrome - ScienceDirect
About MWS - Mowat-Wilson Syndrome Foundation
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
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care | Genetics in Medicine
Mowat-Wilson syndrome: MedlinePlus Genetics
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care | Genetics in Medicine
Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS) - ScienceDirect
Mowat-Wilson syndrome | Journal of Medical Genetics
Photographs of patients with Mowat-Wilson syndrome. Note... | Download Scientific Diagram
Mowat-Wilson Syndrome | Blogs | AmbitCare
Mowat-Wilson syndrome: growth charts | Orphanet Journal of Rare Diseases | Full Text
35. Mowat-Wilson Syndrome - Undergraduate Research
Mowat-Wilson syndrome | Orphanet Journal of Rare Diseases | Full Text
Mowat-Wilson syndrome | Journal of Medical Genetics
Mowat–Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature - Garavelli - 2009 - American Journal of Medical Genetics Part A - Wiley Online Library
The Creation of MowatWilson.org | The University of Chicago Genetic Services
Mowat–Wilson syndrome - Wikipedia
What is Mowat Wilson Syndrome? made incredibly EASY - YouTube
35. Mowat-Wilson Syndrome - Undergraduate Research
Mowat-Wilson syndrome - wikidoc
About MWS - Mowat-Wilson Syndrome Foundation
