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42. [2 cases of a rare association of malformations: microphthalmos and harelip]. Neuschüler R, Santillo C. Boll Ocul; 1967 Dec; 46(12):1022-3. PubMed ID: 5618058 [No Abstract] [Full Text] [Related]
46. Partial trisomy 11,46,XX,-3,-20, + der3, + der20,t(3:11:20), resulting from a complex maternal rearrangement of chromosomes 3, 11, 20. Palmer CG, Poland C, Reed T, Kojetin J. Hum Genet; 1976 Feb 29; 31(2):219-25. PubMed ID: 1248831 [Abstract] [Full Text] [Related]
47. Gross anatomical studies of a newborn with the Meckel syndrome. Pettersen JC. Teratology; 1983 Oct 29; 28(2):157-64. PubMed ID: 6648819 [Abstract] [Full Text] [Related]
53. [Partial trisomy of the short arm of chromosome 3. Case report and phenotype expression]. Frankova YE, Holenova H, Braulke I. Monatsschr Kinderheilkd; 1991 Dec 29; 139(12):841-3. PubMed ID: 1770961 [Abstract] [Full Text] [Related]
57. Trisomy D1 (Patau's syndrome). Masterson JG, Law EM, Donovan DE, O'Brien NG. J Ir Med Assoc; 1968 Jun 29; 61(372):195-200. PubMed ID: 5668668 [No Abstract] [Full Text] [Related]
58. [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)]. Morić-Petrović S, Laća Z, Krajgher A, Milośevic J. Ann Genet; 1976 Sep 29; 19(3):195-7. PubMed ID: 1086628 [Abstract] [Full Text] [Related]