List of works - Karin Dahan

A new informative Alw 26 I polymorphism in exon 10 of the human low density lipoprotein receptor gene. Application to prenatal diagnosis. Mutations in brief no. 145. Online

scientific article published on 01 January 1998

A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension

scientific article published on 01 November 2006

Association of PKD2 (polycystin 2) mutations with left-right laterality defects

scientific article

Belgian consensus statement on the diagnosis and management of patients with atypical hemolytic uremic syndrome.

scientific article

Blau syndrome associated with a CARD15/NOD2 mutation

scientific article

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

scientific article published on 01 September 2019

Frequent mutations of hepatocyte nuclear factor 1 in colorectal cancer with microsatellite instability.

scientific article published in May 2003

From Alport syndrome to benign familial hematuria: clinical and genetic aspect

scientific article

High risk for neoplastic transformation of endometriosis in a carrier of Lynch syndrome

scientific article published in September 2010

Molecular analysis of GB virus C isolates in Belgian hemodialysis patients ⬇️

scientific article published on June 1, 1998

Multiple neoplasia in a 15-year-old girl with familial adenomatous polyposis

scientific article

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

scientific journal article

Outcome of kidney transplantation in type I oral-facial-digital syndrome.

scientific article published on 6 January 2011

Polymicrogyria in chromosome 22q11 deletion syndrome

scientific article published in January 2002

Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in females

scientific article published on 01 December 1995

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

article

List of works by Karin Dahan

A new informative Alw 26 I polymorphism in exon 10 of the human low density lipoprotein receptor gene. Application to prenatal diagnosis. Mutations in brief no. 145. Online

A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension

Association of PKD2 (polycystin 2) mutations with left-right laterality defects

Belgian consensus statement on the diagnosis and management of patients with atypical hemolytic uremic syndrome.

Blau syndrome associated with a CARD15/NOD2 mutation

Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

Frequent mutations of hepatocyte nuclear factor 1 in colorectal cancer with microsatellite instability.

From Alport syndrome to benign familial hematuria: clinical and genetic aspect

High risk for neoplastic transformation of endometriosis in a carrier of Lynch syndrome

Molecular analysis of GB virus C isolates in Belgian hemodialysis patients ⬇️

Multiple neoplasia in a 15-year-old girl with familial adenomatous polyposis

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Outcome of kidney transplantation in type I oral-facial-digital syndrome.

Polymicrogyria in chromosome 22q11 deletion syndrome

Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in females

The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome