Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964)-Reference-Cited by-同舟云学术

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964)

Published:2018-03 Issue: Volume:194 Page:248-252.e2
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Chang Xiao,Li Dong,Tian Lifeng,Liu Yichuan,March Michael,Wang Tiancheng,Hou Cuiping,Pellegrino Renata,Levy Richard,Jen Melinda,Soccio Raymond,Sleiman Patrick,Hakonarson Hakon,Castelo-Soccio Leslie

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference12 articles.

1. The immigration delay disease: adermatoglyphia-inherited absence of epidermal ridges;Burger;J Am Acad Dermatol,2011

2. A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia;Nousbeck;Am J Hum Genet,2011

3. Genome-wide linkage analysis and whole-genome sequencing identify a recurrent SMARCAD1 variant in a unique Chinese family with Basan syndrome;Li;Eur J Hum Genet,2016

4. Analysis of two candidate genes for Basan syndrome;Marks;Am J Med Genet,2014

5. Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14;Lugassy;Am J Hum Genet,2006

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1. Coexistence of Basan syndrome and cutaneous basal cell carcinoma: Genetic and clinical perspectives;The Journal of Dermatology;2024-09-10

2. Basan syndrome in a family from South India: a novel SMARCAD1 variant;Clinical and Experimental Dermatology;2023-11-15

3. Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma;Disease Markers;2022-05-10

4. Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome;American Journal of Medical Genetics Part A;2022-02-25

5. Two SMARCAD1 Variants Causing Basan Syndrome in a Canadian and a Dutch Family;JID Innovations;2021-09