Correction: Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families.

Correction: Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families.

Bibliographic Details
Format:	Article
Language:	English
Published:	Public Library of Science (PLoS) 2014-01-01
Series:	PLoS ONE
Online Access:	http://europepmc.org/articles/PMC4113447

Similar Items

Correction: Mutations in the Homeodomain of HOXD13 Cause Syndactyly Type 1-c in Two Chinese Families
by: The Staff
Published: (2014-01-01)

Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.
by: Limeng Dai, et al.
Published: (2014-01-01)

A 147L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function
by: Caronia, Giuliana
Published: (2002)

Isolated brachydactyly type E caused by a <it>HOXD13 </it>nonsense mutation: a case report
by: Jamsheer Aleksander, et al.
Published: (2012-01-01)

A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family
by: Tahir Zaib, et al.
Published: (2019-12-01)

Evx2-Hoxd13 intergenic region restricts enhancer association to Hoxd13 promoter.
by: Takumi Yamagishi, et al.
Published: (2007-01-01)

Cenani-Lenz syndactyly syndrome - a case report of a family with isolated syndactyly
by: Dineshani Hettiaracchchi, et al.
Published: (2018-07-01)

Cryptophthalmos with syndactyly
by: Sen S
Published: (1976-01-01)

Two Rare Syndromic Syndactyly Cases in Neonates
by: Pooja Prabhakar Kamath
Published: (2021-05-01)

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
by: Najim Lahrouchi, et al.
Published: (2019-03-01)

Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review
by: Roberta Rotunno, et al.
Published: (2021-05-01)

Identification of HOXD4 Mutations in Spinal Extradural Arachnoid Cyst.
by: Yoji Ogura, et al.
Published: (2015-01-01)

Bilateral cryptophthalmos-syndactyly syndrome
by: Gupta G, et al.
Published: (1980-01-01)

Genetic Overview of Syndactyly and Polydactyly
by: Humayun Ahmed, BA, et al.
Published: (2017-11-01)

Mesomelic dysplasias associated with the HOXD locus are caused by regulatory reallocations
by: Christopher Chase Bolt, et al.
Published: (2021-08-01)

New Simple Technique for Syndactyly Release
by: Petra M. Grahn, MD, et al.
Published: (2020-05-01)

Complex Complete Syndactyly In A Child
by: Pedro Martins Branco, et al.
Published: (2019-07-01)

<it>HOXA13 </it>and <it>HOXD13 </it>expression during development of the syndactylous digits in the marsupial <it>Macropus eugenii</it>
by: Chew Keng Yih, et al.
Published: (2012-01-01)

Interactions between members of two homeodomain protein families in Arabidopsis thaliana
by: Pidkowich, Mark Stephen
Published: (2009)

Interactions between members of two homeodomain protein families in Arabidopsis thaliana
by: Pidkowich, Mark Stephen
Published: (2009)

HOXD13 promotes the malignant progression of colon cancer by upregulating PTPRN2
by: Jiangyan Yin, et al.
Published: (2021-08-01)

Hoxd13/Bmp2-mediated mechanism involved in zebrafish finfold design
by: João Castro, et al.
Published: (2021-03-01)

The embryonic genes Dkk3, Hoxd8, Hoxd9 and Tbx1 identify muscle types in a diet-independent and fiber-type unrelated way
by: Boekschoten Mark V, et al.
Published: (2010-03-01)

Study of palmar dermatoglyphic pattern in syndactyly patients
by: M Y Dofe, et al.
Published: (2015-01-01)

Foot Web Space Transfer for Congenital Syndactyly
by: Yoko Katsuragi Tomioka, MD, PhD, et al.
Published: (2020-12-01)

Application of external fixator traction in the treatment of syndactyly
by: Yidong Cui, et al.
Published: (2020-11-01)

Foot Syndactyly: A Clinical and Demographic Analysis
by: Jong Ho Kim, et al.
Published: (2016-11-01)

Hereditary bovine syndactyly in Angus and crossbred cattle
by: Schmidt, Garret L.
Published: (2015)

Tripod-shaped Syndactyly in Apert Syndrome with FGFR2 p.P253R Mutation
by: Chandra Bhan Singh, et al.
Published: (2021-08-01)

Unilateral cryptophthalmos (with syndactyly, laryngeal atresia and genital anomalies)
by: Guhanandhan M, et al.
Published: (1986-01-01)

Clinodactyly and syndactyly – diagnostic clues for Andersen-Tawil syndrome
by: Carlos Andrade, et al.
Published: (2014-11-01)

Synpolydactyly and HOXD13 polyalanine repeat: addition of 2 alanine residues is without clinical consequences
by: Haque Sayedul, et al.
Published: (2007-12-01)

Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency
by: Chih-Ping Chen, et al.
Published: (2017-06-01)

The conservation and divergence of function in the SIX family of homeodomain transcription factors
by: Kitson-Pantano, Raphaëla Joanna
Published: (2008)

Attenuated Acceleration to Leukemia after Ezh2 Loss in Nup98-HoxD13 (NHD13) Myelodysplastic Syndrome
by: Victoria Y. Ling, et al.
Published: (2019-08-01)

Evaluation of the actin architecture in dysplastic megakaryocytes expressing the NUP98-HOXD13 leukemic fusion gene
by: Okyere, Benjamin
Published: (2013)

"Results Of Surgical Treatment Of Syndactyly, Imam Hospital - 1994 To 2003 "
by: Mortazavi, et al.
Published: (2004-09-01)

Macrodystrophia lipomatosa of bilateral hands and the left upper limb with syndactyly
by: Suk Joon Oh
Published: (2019-07-01)

Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation
by: Xiulan Lu, et al.
Published: (2019-02-01)

Correction: Two novel mutations in myosin binding protein C slow causing distal arthrogryposis type 2 in two large Han Chinese families may suggest important functional role of immunoglobulin domain C2.
by: PLOS ONE Staff
Published: (2015-01-01)