Hypertension and brachydactyly syndrome: a further case report-Reference-Cited by-同舟云学术

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Hypertension and brachydactyly syndrome: a further case report

Published:2022-06-27 Issue:4 Volume:31 Page:201-205
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Huang Xiang,Li Xiao-Lan,Liu Fu-Yuan,Li Hao,Zhou Heng,Li Xiao-Mei

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology and Child Health

Reference19 articles.

1. Predicting functional effect of human missense mutations using PolyPhen-2.;Adzhubei;Curr Protoc Hum Genet,2013

2. Phosphodiesterase 3A (PDE3A) deletion suppresses proliferation of cultured murine vascular smooth muscle cells (VSMCs) via inhibition of mitogen-activated protein kinase (MAPK) signaling and alterations in critical cell cycle regulatory proteins.;Begum;J Biol Chem,2011

3. Hereditary brachydactyly associated with hypertension.;Bilginturan;J Med Genet,1973

4. Prediction of post-translational glycosylation and phosphorylation of proteins from the amino acid sequence.;Blom;Proteomics,2004

5. A PDE3A mutation in familial hypertension and brachydactyly syndrome.;Boda;J Hum Genet,2016

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