The Gene for Naegeli–Franceschetti–Jadassohn Syndrome Maps to 17q21-Reference-Cited by-同舟云学术

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The Gene for Naegeli–Franceschetti–Jadassohn Syndrome Maps to 17q21

Published:2000-10 Issue:4 Volume:115 Page:694-698
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Whittock Neil V.,Ashton Gabrielle H.S.,Eady Robin A.J.,McGrath John A.,Coleman Carrie M.,Irwin McLean W.H.,Acland K.M.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference33 articles.

1. Structure and chromosomal location of the human granulin gene;Bhandari;Biochem Biophys Res Commun,1992

2. Isolation and sequence of the granulin precursor cDNA from human bone marrow reveals tandem cysteine-rich granulin domains;Bhandari;Proc Natl Acad Sci USA,1992

3. Mutation of a type II keratin gene (K6a) in pachyonychia congenita;Bowden;Nat Genet,1995

4. Comprehensive human genetic maps: individual and sex-specific variation in recombination;Broman;Am J Hum Genet,1998

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Naegeli–Franceschetti–Jadassohn Syndrome: A Rare Case of Entwine Hue of Pigmentary World;Indian Journal of Paediatric Dermatology;2024-04

2. Naegeli–Franceschetti–Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT 14 frameshift variant;British Journal of Dermatology;2019-07-15

3. Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder;Indian Journal of Dermatology;2019

4. Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders;Dermatology Research and Practice;2017

5. A Novel Locus for Ectodermal Dysplasia of Hair, Nail and Skin Pigmentation Anomalies Maps to Chromosome 18p11.32-p11.31;PLOS ONE;2015-06-26

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