Twin brothers with MIDAS syndrome and XX karyotype
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. Abstracts of the meeting of the Clinical Genetics Society held on 7 and 8 April 1988 at the University of Oxford
2. Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.
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4. Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): A clue to the pathogenesis of oncocytic cardiomyopathy?
5. Xp22.3; Yq11.2 chromosome translocation and its clinical manifestations
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1. Translocation t(X;Y) characterized by chromosomal microarray and FISH in a phenotypic male with Microphthalmia and linear skin defects;Clinical Dysmorphology;2023-11-11
2. MIDAS Syndrome (Microphthalmia with Linear Skin Defects);Neurocutaneous Disorders;2022
3. Linear Skin Defects with Multiple Congenital Anomalies (LSDMCA): An Unconventional Mitochondrial Disorder;Genes;2021-02-11
4. Microphthalmia with linear skin defects syndrome associated with hypopigmented mosaic lesions and ptosis: two siblings from Africa;International Journal of Dermatology;2020-05-09
5. Linear skin defects and microphthalmia;Clinical and Experimental Dermatology;2018-06-12
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