| P2093 | author name string | P Morville | |
| | N Bednarek | |
| | C Eschard | |
| | L Kherbaoui-Redouani | |
| P2860 | cites work | Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome | Q32129470 |
| | Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3. | Q33596996 |
| | MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome | Q34346787 |
| | Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): a clue to the pathogenesis of oncocytic cardiomyopathy? | Q40593553 |
| | Xp microdeletion syndrome characterized by pathognomonic linear skin defects on the head and neck | Q41364340 |
| | Another observation of microphthalmia in an XX male: microphthalmia with linear skin defects syndrome without linear skin lesions | Q48764568 |
| | Reticulolinear aplasia cutis congenita of the face and neck: a distinctive cutaneous manifestation in several syndromes linked to Xp22. | Q52184288 |
| | Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. | Q52219104 |
| | Linear facial skin defects associated with microphthalmia and other malformations, with chromosome deletion Xp22.1. | Q72197023 |
| | Second 46,XX male with MLS syndrome | Q74329284 |
| P433 | issue | 3 | |
| P304 | page(s) | 224-226 | |
| P577 | publication date | 2003-03-01 | |
| P1433 | published in | Archives de Pediatrie | Q15757206 |
| P1476 | title | [Cutaneous aplasia, non compaction of the left ventricle and severe cardiac arrhythmia: a new case of MLS syndrome (microphtalmia with linear skin defects)] | |
| P478 | volume | 10 | |