Microphthalmia with linear skin defects (MLS) syndrome evaluated by prenatal karyotyping, FISH and array comparative genomic hybridization
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference26 articles.
1. Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.
2. Twin brothers with MIDAS syndrome and XX karyotype
3. X-chromosome methylation ratios as indicators of chromosomal activity: Evidence of intraindividual divergencies among tissues of different embryonal origin
4. Overlapping Specificities of the Mitochondrial Cytochrome c and c1 Heme Lyases
5. Phenotypic Variation in Ophthalmic Manifestations of MIDAS Syndrome(Microphthalmia, Dermal Aplasia, and Sclerocornea)
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Linear Skin Defects with Multiple Congenital Anomalies (LSDMCA): An Unconventional Mitochondrial Disorder;Genes;2021-02-11
2. Syndromic Eye Anomalies;Fetal and Neonatal Eye Pathology;2020
3. Anterior Segment Developmental Anomalies in a 33-Week-Old Fetus with MIDAS Syndrome;Pediatric and Developmental Pathology;2014-11
4. MIDAS (microphthalmia, dermal aplasia, sclerocornea) syndrome with central nervous system abnormalities;Clinical Dysmorphology;2009-10
5. Microphthalmia with Linear Skin Defects: A Case Report and Review;Pediatric Dermatology;2008-09
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