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Journal Abstract Search
91 related items for PubMed ID: 612923
1. [Orofaciodigital syndrome (types I and II)]. Fukuyama Y. Nihon Rinsho; 1977; 35 Suppl 1():622-3. PubMed ID: 612923 [No Abstract] [Full Text] [Related]
8. Bartsocas-Papas syndrome. A case report. Cheirif S, Grayson BH, Maccaro HA. N Y State Dent J; 1985 Feb; 51(2):101-2. PubMed ID: 2984611 [No Abstract] [Full Text] [Related]
9. [Orofaciodigital syndrome type I in a mother and daughter]. Guerrero Vázquez J, Cazenave Bernal A, de Paz Aparicio P, Luengo Casasola JL, Garcés Ramos A, López Vázquez JL, Hoyos Madrid JJ. An Esp Pediatr; 1988 Jan; 28(1):59-62. PubMed ID: 3279888 [Abstract] [Full Text] [Related]
10. [Coffin-Lowry syndrome. Description of 2 cases]. Barajas LO, Rivera H, Fragoso R, Nazara Z, Cantú JM. Bol Med Hosp Infant Mex; 1986 Jun; 43(6):378-81. PubMed ID: 3730116 [No Abstract] [Full Text] [Related]
11. Coffin-Lowry syndrome in an Afro-American family. Kousseff BG. Am J Med Genet; 1982 Mar; 11(3):373-5. PubMed ID: 7081302 [No Abstract] [Full Text] [Related]
12. [Oto-palato-digital type I syndrome in five generations. Relationship to the type II form]. Le Marec B, Odent S, Bracq E, Bulard MB, Bourdinière J, Babut JM. Ann Genet; 1988 Mar; 31(3):155-61. PubMed ID: 3265608 [Abstract] [Full Text] [Related]
13. [Brachmann-Cornelia de Lange syndrome]. Bonioli E, Bellini C, Ruffa G, Camera G, Gemme G. Minerva Pediatr; 1987 Feb 28; 39(3-4):135-8. PubMed ID: 3587191 [No Abstract] [Full Text] [Related]
14. Orofaciodigital syndrome type IV: report of a patient. Nevin NC, Thomas PS. Am J Med Genet; 1989 Feb 28; 32(2):151-4. PubMed ID: 2929654 [Abstract] [Full Text] [Related]
15. [Freeman-Sheldon syndrome. Description of 2 cases of probable recessive autosomal inheritance]. Bonioli E, Bellini C, Ruffa G, Lagorio V, Gemme G. Minerva Pediatr; 1987 Feb 28; 39(3-4):123-7. PubMed ID: 3587189 [No Abstract] [Full Text] [Related]
16. [Aarskog's syndrome. Description of a familial case]. Tucciarone L, De Santis F, Ballati G, Latini M, Felici W. Minerva Pediatr; 1987 Apr 30; 39(8):341-6. PubMed ID: 3614163 [No Abstract] [Full Text] [Related]
18. Discordance in monozygotic twins for aglossia-adactylia, and possible clues to the pathogenesis of the syndrome. Robinow M, Marsh JL, Edgerton MT, Sabio H, Johnson GF. Birth Defects Orig Artic Ser; 1978 Apr 30; 14(6A):223-30. PubMed ID: 569511 [No Abstract] [Full Text] [Related]
19. [A new genetic variant of the orofaciodigital syndrome]. Bochkova DN, Ternova TI. Pediatriia; 1990 Apr 30; (3):95-6. PubMed ID: 2385482 [No Abstract] [Full Text] [Related]