These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
243 related items for PubMed ID: 7246606
21. Diagnostic precision in microphthalmos and coloboma of heterogeneous origin. Warburg M. Birth Defects Orig Artic Ser; 1982; 18(6):31-50. PubMed ID: 7171763 [Abstract] [Full Text] [Related]
23. BBBG syndrome or Opitz syndrome: new family. Verloes A, Le Merrer M, Briard ML. Am J Med Genet; 1989 Nov; 34(3):313-6. PubMed ID: 2688419 [Abstract] [Full Text] [Related]
24. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome. Baraitser M, Winter RM. J Med Genet; 1988 Jan; 25(1):41-3. PubMed ID: 3351890 [Abstract] [Full Text] [Related]
25. Ocular hypotelorism, submucosal cleft palate, and hypospadias: a new autosomal dominant syndrome. Schilbach U, Rott HD. Am J Med Genet; 1988 Dec; 31(4):863-70. PubMed ID: 3149147 [Abstract] [Full Text] [Related]
26. Silver staining of the supernumerary chromosome in the cat-eye syndrome. Petit P, Godart S, Fryns JP. Ann Genet; 1980 Dec; 23(2):114-6. PubMed ID: 6156636 [Abstract] [Full Text] [Related]
27. The "cat eye" syndrome--report of a case with hypothyroidism. Ioan D, Dumitriu L, Fabriţius K, Simescu M, Maximilian C. Endocrinologie; 1986 Dec; 24(2):129-31. PubMed ID: 3738402 [Abstract] [Full Text] [Related]
28. Iris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2. Pallotta R. J Med Genet; 1991 May; 28(5):342-4. PubMed ID: 1865474 [Abstract] [Full Text] [Related]
29. Autosomal dominant piebaldism and mental retardation syndrome associated with a t(1;2) (p22.1;q36). Rivera H, Alvarez-Arratia MC, Moller M, Tinoco-Contreras M, Flores-Perez A, Cantu JM. J Genet Hum; 1986 Aug; 34(3-4):321-5. PubMed ID: 3760835 [Abstract] [Full Text] [Related]
30. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1. Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY. Invest Ophthalmol Vis Sci; 2002 Aug; 43(8):2540-5. PubMed ID: 12147582 [Abstract] [Full Text] [Related]
31. Brief clinical report: dup(4p15 leads to 4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation. Clark CE, Telfer MA, Cowell HR, Kalamchi A, Steg NL. Am J Med Genet; 1982 Jan; 11(1):37-42. PubMed ID: 7065001 [Abstract] [Full Text] [Related]
32. The Marinesco-Sjögren syndrome: polygraphic study of nocturnal sleep. Bramanti P, Ricci RM, Benedetto M, Candela L, Bagalà S, Di Perri R. Acta Neurol (Napoli); 1985 Feb; 7(1):8-13. PubMed ID: 3993461 [No Abstract] [Full Text] [Related]
34. G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias-dysphagia, or "Opitz-Frias" or "Opitz-G" syndrome)--perspective in 1987 and bibliography. Opitz JM. Am J Med Genet; 1987 Oct; 28(2):275-85. PubMed ID: 3322001 [No Abstract] [Full Text] [Related]
35. De novo ring chromosome 3 in a girl with hypoplastic thumb and coloboma of iris. Barajas-Barajas LO, Velarde-Félix S, Elizarrarás-Rivas J, Hernández-Zaragoza G, Vázquez-Herrera JA. Genet Couns; 2001 Oct; 12(2):151-6. PubMed ID: 11491310 [Abstract] [Full Text] [Related]
36. SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma. Gregory-Evans CY, Moosajee M, Hodges MD, Mackay DS, Game L, Vargesson N, Bloch-Zupan A, Rüschendorf F, Santos-Pinto L, Wackens G, Gregory-Evans K. Hum Mol Genet; 2007 Oct 15; 16(20):2482-93. PubMed ID: 17656375 [Abstract] [Full Text] [Related]
37. [Familial occurrence of congenital aniridia]. Zalewska R, Midro AT, Bakunowicz-Lazarczyk A, Proniewska-Skretek E. Klin Oczna; 1992 Oct 15; 94(5-6):159-60. PubMed ID: 1453680 [Abstract] [Full Text] [Related]
38. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion. Wieczorek D, Krause M, Majewski F, Albrecht B, Horn D, Riess O, Gillessen-Kaesbach G. Eur J Hum Genet; 2000 Jul 15; 8(7):519-26. PubMed ID: 10909852 [Abstract] [Full Text] [Related]
39. Autosomal dominant typical coloboma associated with unilateral pseudoptosis, myopia and cataract. Porges Y. Cent Afr J Med; 1995 Aug 15; 41(8):255-7. PubMed ID: 7585914 [Abstract] [Full Text] [Related]