Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23

Publisher： Karger

E-ISSN： 1424-859x|86|3-4|296-304

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.86, Iss.3-4, 1999-11, pp. : 296-304

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23

By  

Cytogenetic and Genome Research, Vol. 82, Iss. 3-4, 1998-12 ,pp. : 238-246

Karger

Access to resources Recommend Favorite

Induced Chromosome Deletion in a Williams-Beuren Syndrome Mouse Model Causes Cardiovascular Abnormalities

By  

Journal of Vascular Research, Vol. 48, Iss. 2, 2010-10 ,pp. : 119-129

Karger

Access to resources Recommend Favorite

Spontaneous Intracerebral Hemorrhage and Multiple Infarction in Williams-Beuren Syndrome

By  

Pediatric Neurosurgery, Vol. 39, Iss. 6, 2004-01 ,pp. : 335-338

Karger

Access to resources Recommend Favorite

P14.02: Ultrasound features in a case of Williams‐Beuren syndrome at second trimester scan

By  

ULTRASOUND IN OBSTETRICS & GYNECOLOGY, Vol. 46, Iss. S1, 2015-09 ,pp. : 164-165

John Wiley & Sons Inc

Access to resources Recommend Favorite

Williams-Beuren Syndrome: Experience of 43 Patients and a Report of an Atypical Case from a Tertiary Care Center in India

By  

Cytogenetic and Genome Research, Vol. 146, Iss. 3, 2015-0 ,pp. : 187-194

Karger

Access to resources Recommend Favorite