▷ ICD10 code of Mowat-Wilson syndrome and ICD9 code
Characterisation of deletions of the ZFHX1B region and genotype-phenotype analysis in Mowat-Wilson syndrome | Journal of Medical Genetics
Mowat-Wilson syndrome: MedlinePlus Genetics
Novel Zeb2 gene variation in the Mowat Wilson syndrome (MWS) - ScienceDirect
Brady - Mowat-Wilson Syndrome Foundation
PDF) Mowat-Wilson Syndrome as a Differential Diagnosis in Patients with Congenital Heart Defects and Dysmorphic Facies
Figure 1 from ZEB2 Gene Mutation and Duplication of 22q11.23 in Mowat-Wilson Syndrome | Semantic Scholar
Mowat-Wilson syndrome - wikidoc
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
Mowat-Wilson syndrome: MedlinePlus Genetics
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
Mowat-Wilson Syndrome OMIM# 235730 - FDNA™
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
MOWAT-WILSON SYNDROME FOUNDATION - GuideStar Profile
HELP HIM REACH HIS NEXT STEP – GOAL R 10 000 - Click 'n Donate, Fundraising South Africa, for South Africans
The Creation of MowatWilson.org | The University of Chicago Genetic Services
Isabella - Mowat-Wilson Syndrome Foundation
Mowat–Wilson syndrome - Wikipedia
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care | Genetics in Medicine