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24. [Congenital dislocations of the major joints, multiple bone abnormalities and typical facial structure (Larsen's syndrome)]. Szabó L; Perjés K Magy Traumatol Orthop Helyreallito Seb; 1974 Jan; 17(1):37-42. PubMed ID: 4150845 [No Abstract] [Full Text] [Related]
25. MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome. Happle R; Daniëls O; Koopman RJ Am J Med Genet; 1993 Oct; 47(5):710-3. PubMed ID: 8267001 [TBL] [Abstract][Full Text] [Related]
26. Anterior chamber cleavage syndrome. A typical case of Peters' anomaly with primary aphakia. Holmark J; Jensen OA Acta Ophthalmol (Copenh); 1972; 50(6):877-86. PubMed ID: 4631516 [No Abstract] [Full Text] [Related]
27. Corneal opacities in the Hallermann-Streiff syndrome. Roulez FM; Schuil J; Meire FM Ophthalmic Genet; 2008 Jun; 29(2):61-6. PubMed ID: 18484310 [TBL] [Abstract][Full Text] [Related]
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29. A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report. Hu Q; Mai J; Xiang Q; Zhou B; Liu S; Wang J BMC Pediatr; 2022 Feb; 22(1):82. PubMed ID: 35130870 [TBL] [Abstract][Full Text] [Related]
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31. [Eugenic counseling after a birth of an infant with congenital malformations]. Beolchini PE Minerva Med; 1972 Nov; 63(85):4660-4. PubMed ID: 4264406 [No Abstract] [Full Text] [Related]
33. Ocular manifestations of congenital rubella syndrome in a developing country. Vijayalakshmi P; Kakkar G; Samprathi A; Banushree R Indian J Ophthalmol; 2002 Dec; 50(4):307-11. PubMed ID: 12532496 [TBL] [Abstract][Full Text] [Related]
34. A variant of the cerebro-oculo-facio-skeletal syndrome with congenital ectropion and a case of lamellar ichthyosis in the same family. Stratakis CA; Runkle B; Rennert OM Clin Genet; 1994 Mar; 45(3):162-3. PubMed ID: 8026108 [No Abstract] [Full Text] [Related]
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