CrossRef Text and Data Mining
Result of CrossRef Text and Data Mining Search is the related articles with entitled article. If you click link1 or link2 you will be able to reach the full text site of selected articles; however, some links do not show the full text immediately at now. If you click CrossRef Text and Data Mining Download icon, you will be able to get whole list of articles from literature included in CrossRef Text and Data Mining.
Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
Olfa Hdiji, Emna Turki, Nouha Bouzidi, Imen Bouchhima, Mariem Damak, Saeed Bohlega, Chokri Mhiri
JMD. 2016;9(2):120-123.   Published online 2016 May 25    DOI: https://doi.org/10.14802/jmd.16003

Excel Download

Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation
Journal of Movement Disorders. 2016;9(2):120-123   Crossref logo
Link1 Link2 Link3

A novel splice site mutation in gene C2orf37 underlying Woodhouse–Sakati syndrome (WSS) in a consanguineous family of Pakistani origin
Gene. 2011;490(1-2):26-31   Crossref logo
Link1 Link2

A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome
Clinical Genetics. 2010;78(6):594-597   Crossref logo
Link1

Phenotypic heterogeneity in Woodhouse-Sakati syndrome: Two new families with a mutation in the C2orf37 gene
American Journal of Medical Genetics Part A. 2011;155(11):2647-2653   Crossref logo
Link1 Link2

Woodhouse–Sakati syndrome in a family is associated with a homozygous start loss mutation in the DCAF 17 gene
Clinical and Experimental Dermatology. 2019;45(2):159-164   Crossref logo
Link1 Link2 Link3 Link4

Alopecia and Hypotrichosis as Characteristic Findings in Woodhouse-Sakati Syndrome: Report of a Family with Mutation in theC2orf37Gene
Pediatric Dermatology. 2013;31(1):83-87   Crossref logo
Link1

Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse–Sakati syndrome
Journal of Genetics. 2015;94(3):489-492   Crossref logo
Link1 Link2 Link3

C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients
Clinical Genetics. 2010;78(6):585-590   Crossref logo
Link1

Dystonia in the Woodhouse Sakati syndrome: A new family and literature review
Movement Disorders. 2008;23(4):592-596   Crossref logo
Link1 Link2

Japanese siblings with woodhouse-sakati syndrome: The first family in East Asia
Journal of the Neurological Sciences. 2017;381:457   Crossref logo
Link1 Link2

This metadata service is kindly provided by CrossRef from May 29, 2014. JMD has participated in CrossRef Text and Data Mining service since October 29, 2014.