Pathogenic copy number variants in patients with congenital hypopituitarism associated with complex phenotypes

Publisher： John Wiley & Sons Inc

E-ISSN： 1365-2265|88|3|425-431

ISSN： 0300-0664

Source： CLINICAL ENDOCRINOLOGY, Vol.88, Iss.3, 2018-03, pp. : 425-431

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

Copy number variation in metabolic phenotypes

By  

Cytogenetic and Genome Research, Vol. 123, Iss. 1-4, 2009-03 ,pp. : 169-175

Karger

Access to resources Recommend Favorite

PAX6 allelic heterogeneity in Mexican congenital aniridia patients: expanding the mutational spectrum with seven novel pathogenic variants

By  

CLINICAL & EXPERIMENTAL OPHTHALMOLOGY, Vol. 45, Iss. 9, 2017-12 ,pp. : 875-883

John Wiley & Sons Inc

Access to resources Recommend Favorite

Analysis of Germline Gene Copy Number Variants of Patients with Sporadic Pancreatic Adenocarcinoma Reveals Specific Variations

By  

Oncology, Vol. 85, Iss. 5, 2013-11 ,pp. : 306-311

Karger

Access to resources Recommend Favorite

Identification of Copy Number Variants on Human Chromosome 22 in Patients with a Variety of Clinical Findings

By  

Cytogenetic and Genome Research, Vol. 134, Iss. 4, 2011-08 ,pp. : 260-268

Karger

Access to resources Recommend Favorite

Subtelomeric Copy Number Variations: The Importance of 4p/4q Deletions in Patients with Congenital Anomalies and Developmental Disability

By  

Cytogenetic and Genome Research, Vol. 149, Iss. 4, 2016-09 ,pp. : 241-246

Karger

Access to resources Recommend Favorite