X‐linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations-Reference-Cited by-同舟云学术

X‐linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations

Published:2020-01-16 Issue:5 Volume:34 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Zhang Min¹^ORCID,Huang Hailong¹^ORCID,Lin Na¹,He Shuqiong¹,An Gang¹,Wang Yan¹,Chen Meihuan¹^ORCID,Chen Lingji¹,Lin Yuan¹,Xu Liangpu¹

Affiliation:

1. Fujian Key Laboratory for Prenatal Diagnosis and Birth Defect Fujian Maternity and Child Health Hospital Affiliated Hospital of Fujian Medical University Fuzhou China

Funder

the Key Clinical Specialty Discipline Construction Program of Fujian

the Key Special Projects of Fujian Provincial Department of Science and Technology

the Fujian Provincial Natural Science Foundation

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.23201

Reference28 articles.

1. Die nichtsyndromalen Ichthyosen - aktueller Stand

2. Prevalence of steroid sulfatase deficiency in California according to race and ethnicity

3. Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols

4. X-linked ichthyosis: An oculocutaneous genodermatosis

5. Inherited ichthyosis: Non-syndromic forms

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