MIDAS syndrome respectively MLS syndrome: A separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome-Reference-Cited by-同舟云学术

MIDAS syndrome respectively MLS syndrome: A separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome

Published:1995-05-22 Issue:1 Volume:57 Page:117-118
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Mücke J.,Happle R.,Theile H.

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.1320570123

Reference3 articles.

1. MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): An X‐linked phenotype distinct from Goltz syndrome

2. Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization

3. MuckeJ(1994): MIDAS syndrome (microphthalmia dermal aplasia and sclerocornea): An autonomous entity with linear skin defects within the spectrum of dermal hypoplasias.Eur J Dermatolin press.

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