Hair loss, facial dysmorphology, and skeletal alterations – a diagnostic challenge-Reference-Cited by-同舟云学术

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Hair loss, facial dysmorphology, and skeletal alterations – a diagnostic challenge

Published:2021-06-20 Issue:10 Volume:60 Page:
ISSN:0011-9059
Container-title:International Journal of Dermatology
language:en
Short-container-title:Int J Dermatol

Author:

Kondo Rogério Nabor¹,Basmanav Fitnat Buket²,Wolf Sabrina²,Minelli Lorivaldo¹,Frank Jorge³,Betz Regina C.²

Affiliation:

1. Dermatology Service Hospital Universitário Regional do Norte do Paraná State University of Londrina Paraná Brazil

2. Institute of Human Genetics University of Bonn Medical Faculty & University Hospital Bonn Bonn Germany

3. Department of Dermatology, Venereology and Allergology University Medical Center Göttingen Göttingen Germany

Funder

German-Israeli Foundation for Scientific Research and Development

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Dermatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijd.15718

Reference5 articles.

1. Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I

2. Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome

3. Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes

4. Tricho‐rhino‐phalangeal syndrome;Giedion A;Helv Paediatr Acta,1966

5. Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

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