Hirschsprung’s disease in children with Mowat–Wilson syndrome

Mowat-Wilson syndrome: neurological and molecular study in seven patients

(2015) José Albino da Paz et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases

(2014) Tara L. Wenger et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

The spectrum ofZEB2mutations causing the Mowat-Wilson syndrome in Japanese populations

(2014) Yasukazu Yamada et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

ZEB2 Gene Mutation and Duplication of 22q11.23 in Mowat-Wilson Syndrome

(2014) Ersida Buraniqi et al.   JOURNAL OF CHILD NEUROLOGY

Extensive clinical, hormonal and genetic screening in a large consecutive series of 46,XY neonates and infants with atypical sexual development

(2014) Dorien Baetens et al.   Orphanet Journal of Rare Diseases

ZEB2, a new candidate gene for asplenia

(2014) Linda Pons et al.   Orphanet Journal of Rare Diseases

The association between Hirschsprung’s disease and multiple endocrine neoplasia type 2a: a systematic review

(2014) David Coyle et al.   PEDIATRIC SURGERY INTERNATIONAL

Mowat–Wilson syndrome: the first report of an association with central nervous system tumors

(2013) Elvis Terci Valera et al.   CHILDS NERVOUS SYSTEM

Ocular phenotype of Mowat–Wilson syndrome in the first reported Cypriot patients

(2013) George A. Tanteles et al.   CLINICAL DYSMORPHOLOGY

Mowat–Wilson syndrome detected by using high resolution microarray

(2013) Jae Young Park et al.   GENE

ZEB2 zinc-finger missense mutations lead to hypomorphic alleles and a mild Mowat–Wilson syndrome

(2013) Jamal Ghoumid et al.   HUMAN MOLECULAR GENETICS

Mowat-Wilson Syndrome

(2013) Ebtesam Mohamed Abdalla et al.   JOURNAL OF CHILD NEUROLOGY

Hirschsprung’s disease associated with Down syndrome: a meta-analysis of incidence, functional outcomes and mortality

(2013) Florian Friedmacher et al.   PEDIATRIC SURGERY INTERNATIONAL

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

(2012) U Tacke et al.   NEUROPEDIATRICS

Ophthalmologic Abnormalities in Mowat-Wilson Syndrome and a Mutation inZEB2

(2012) Michelle Ariss et al.   OPHTHALMIC GENETICS

Chromosomal and related Mendelian Syndromes associated with Hirschsprung’s disease

(2012) S. W. Moore   PEDIATRIC SURGERY INTERNATIONAL

Clinical utility gene card for: Mowat–Wilson syndrome

(2011) Marcella Zollino et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Avoiding Pitfalls in Molecular Genetic Testing

(2011) Michael Joseph Kluk et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Intrahepatic Biliary Anomalies in a Patient With Mowat-Wilson Syndrome Uncover a Role for the Zinc Finger Homeobox Gene zfhx1b in Vertebrate Biliary Development

(2011) Shuang Cui et al.   JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION

Mowat-Wilson syndrome with associated dysphagia

(2010) Eloise J. Prijoles et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Severe clinical course of Hirschsprung disease in a Mowat-Wilson syndrome patient

(2010) R. Smigiel et al.   JOURNAL OF APPLIED GENETICS

Supernumerary Intestinal Muscle Coat in a Patient with Hirschsprung Disease/Mowat-Wilson Syndrome

(2010) May Leong et al.   PEDIATRIC AND DEVELOPMENTAL PATHOLOGY

Hirschsprung's disease

(2010) Simon E. Kenny et al.   Seminars in Pediatric Surgery

Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature

(2009) L. Garavelli et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mowat-Wilson syndrome: an underdiagnosed syndrome?

(2009) E Engenheiro et al.   CLINICAL GENETICS

Outcomes of Hirschsprung's disease associated with Mowat-Wilson syndrome

(2009) Arnaud Bonnard et al.   JOURNAL OF PEDIATRIC SURGERY

Safe use of the classic laryngeal mask airway and endotracheal intubation in general anaesthesia for a patient with Mowat-Wilson syndrome

(2009) Fiona Kiernan et al.   PEDIATRIC ANESTHESIA

Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in theZEB2gene

(2008) Massimiliano Cecconi et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mowat–Wilson syndrome: the clinical report with the novel mutation in ZFHX1B (exon 8: c.2372del C; p.T791fsX816)

(2008) Antun Sasso et al.   CHILDS NERVOUS SYSTEM

Mowat-Wilson Syndrome Affecting 3 Siblings

(2008) Motoko Ohtsuka et al.   JOURNAL OF CHILD NEUROLOGY