List of works - Nurten A Akarsu

A Large Family with Type IV Radial Polydactyly ⬇️

scientific article published on August 1, 1998

A large Turkish kindred with syndactyly type II (synpolydactyly). 1. Field investigation, clinical and pedigree data ⬇️

scientific article published on June 1, 1995

A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype? ⬇️

scientific article published on June 1, 1995

CRIM1 haploinsufficiency causes defects in eye development in human and mouse

scientific article

Genetic linkage study of familial Mediterranean fever (FMF) to 16p13.3 and evidence for genetic heterogeneity in the Turkish population ⬇️

scientific article published on July 1, 1997

Intracranial and Extracranial Malformations in Patients With Craniofacial Anomalies ⬇️

scientific article published on September 1, 2010

Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker ⬇️

scientific article published on August 1, 1995

Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling

scientific article published on 27 July 2016

Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a U2HR mutation ⬇️

scientific article published on 01 October 2010

Mutation in Exon 1f of PLEC, Leading to Disruption of Plectin Isoform 1f, Causes Autosomal-Recessive Limb-Girdle Muscular Dystrophy ⬇️

scientific article published on November 25, 2010

Mutations affecting the BHLHA9 DNA-binding domain cause MSSD, mesoaxial synostotic syndactyly with phalangeal reduction, Malik-Percin type

scientific article

Mutations in RIPK4 Cause the Autosomal-Recessive Form of Popliteal Pterygium Syndrome ⬇️

scientific article published on December 22, 2011

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like features

scientific article published on 3 October 2017

Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association

scientific article published on 15 October 2015

Sequence Analysis and Homology Modeling Suggest That Primary Congenital Glaucoma on 2p21 Results from Mutations Disrupting Either the Hinge Region or the Conserved Core Structures of Cytochrome P4501B1 ⬇️

scientific article published on March 1, 1998

Smaller Hippocampus Volume Is Associated with Short Variant of 5-HTTLPR Polymorphism in Medication-Free Major Depressive Disorder Patients ⬇️

scientific article published on October 20, 2010

List of works by Nurten A Akarsu