Genetic Signature of Acute Lymphoblastic Leukemia and Netherton Syndrome Co-incidence—First Report in the Literature-Reference-Cited by-同舟云学术

Genetic Signature of Acute Lymphoblastic Leukemia and Netherton Syndrome Co-incidence—First Report in the Literature

Published:2020-01-17 Issue: Volume:9 Page:
ISSN:2234-943X
Container-title:Frontiers in Oncology
language:
Short-container-title:Front. Oncol.

Author:

Skoczen Szymon,Stepien Konrad,Mlynarski Wojciech,Centkowski Piotr,Kwiecinska Kinga,Korostynski Michal,Piechota Marcin,Wyrobek Elzbieta,Moryl-Bujakowska Angelina,Strojny Wojciech,Rej Magdalena,Kowalczyk Jerzy,Balwierz Walentyna

Publisher

Frontiers Media SA

Subject

Cancer Research,Oncology

Reference42 articles.

1. Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping;Chavanas;Am J Hum Genet.,2000

2. Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome;Chavanas;Nat Genet.,2000

3. Netherton syndrome: a genotype-phenotype review;Sarri;Mol Diagn Ther.,2017

4. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009;Oji;J Am Acad Dermatol.,2010

5. Genome instability syndromes caused by impaired DNA repair and aberrant DNA damage responses;Terabayashi;Cell Biol Toxicol.,2018

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1. Netherton Syndrome with a Novel Likely Pathogenic Variant c.420del (p.Ser141ProfsTer5) in SPINK5 Gene: A Case Report;Case Reports in Dermatology;2024-02-23

2. Genetic background assessment with whole exome sequencing in a giant coronary artery ectasia: A pilot study;Kardiologia Polska;2023-10-16

3. Biochemical and Hematologic Profiles in B-Cell Acute Lymphoblastic Leukemia Children;Journal of Pediatric Hematology/Oncology;2023-07-14

4. Genetic Counseling Challenges: A Case Report of a 6-Year-Old Child with Developmental Delay and B-Acute Lymphoblastic Leukemia;Apollo Medicine;2023-06-09

5. A novel mutation in SPINK5 gene underlies a case of atypical Netherton syndrome;Frontiers in Genetics;2022-09-09