Literature DB >> 31567426

Dual genetic diagnoses: neurofibromatosis type 1 and KBG syndrome.

Paola Cianci1, Laura Pezzoli2, Silvia Maitz3, Massimo Agosti1, Maria Iascone2, Angelo Selicorni4.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2020        PMID： 31567426     DOI： 10.1097/MCD.0000000000000296

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


× No keyword cloud information.
  2 in total

1.  Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients.

Authors:  Erica Rosina; Lidia Pezzani; Laura Pezzoli; Daniela Marchetti; Matteo Bellini; Alba Pilotta; Olga Calabrese; Emanuele Nicastro; Francesco Cirillo; Anna Cereda; Agnese Scatigno; Donatella Milani; Maria Iascone
Journal:  Genes (Basel)       Date:  2022-07-19       Impact factor: 4.141

2.  Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the Literature.

Authors:  Fenqi Gao; Xiu Zhao; Bingyan Cao; Xin Fan; Xiaoqiao Li; Lele Li; Shengbin Sui; Zhe Su; Chunxiu Gong
Journal:  J Pers Med       Date:  2022-03-05
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.