scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0002-9394(14)76861-8 |
P698 | PubMed publication ID | 1951596 |
P2093 | author name string | R A Lewis | |
F Greenberg | |||
J R Patrinely | |||
M A De La Paz | |||
L Merin | |||
P2860 | cites work | Aniridia associated with microcornea and subluxated lenses | Q33650565 |
Craniosynostosis and lid anomalies: report of a girl with Michels syndrome | Q34259643 | ||
Anatomical classification facial, cranio-facial and latero-facial clefts | Q34342797 | ||
Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients | Q34685121 | ||
A clefting syndrome with ocular anterior chamber defect and lid anomalies | Q55989759 | ||
Frontofacionasal dysplasia: evidence for autosomal recessive inheritance | Q70509299 | ||
Strabismus in ptosis | Q71232135 | ||
Blepharoptosis, Blepharophimosis, Epicanthus Inversus, and Telecanthus—A Syndrome by No Name | Q71819002 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 572-580 | |
P577 | publication date | 1991-11-01 | |
P1433 | published in | American Journal of Ophthalmology | Q4744258 |
P1476 | title | A sibship with unusual anomalies of the eye and skeleton (Michels' syndrome) | |
P478 | volume | 112 |
Q72733476 | Autosomal dominant inheritance of iridogoniodysgenesis and cataract |
Q24607800 | MASP1 mutations in patients with facial, umbilical, coccygeal, and auditory findings of Carnevale, Malpuech, OSA, and Michels syndromes |
Q40483750 | Michels syndrome in a Brazilian girl born to consanguineous parents |
Q34574645 | Michels syndrome: the first case report from India and review of literature |