A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q-Reference-Cited by-同舟云学术

A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q

Published:2017-04 Issue:4 Volume:60 Page:224-227
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Sirchia Fabio^ORCID,Di Gregorio Eleonora,Restagno Gabriella,Grosso Enrico,Pappi Patrizia,Talarico Flavia,Savin Elisa,Cavalieri Simona,Giorgio Elisa,Mancini Cecilia,Pasini Barbara,Mehta Jodhbir S.,Brusco Alfredo^ORCID

Funder

MURST

Wellcome Trust

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference17 articles.

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1. A MIR17HG-derived long noncoding RNA provides an essential chromatin scaffold for protein interaction and myeloma growth;Blood;2023-01-26

2. Novel Mutations Identified in the Chinese Han Population with Keratoconus by Next-Generation Sequencing;Journal of Ophthalmology;2022-02-10

3. First Patient Diagnosed as Feingold Syndrome Type 2 with Alport Syndrome and Review of the Current Literature;Molecular Syndromology;2022

4. Keratoconus in a child with partial trisomy 13;Ophthalmic Genetics;2021-04-16

5. Feingold syndrome type 2 in a patient from China;American Journal of Medical Genetics Part A;2021-04-05