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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
236 related items for PubMed ID: 144680
41. [Libernan-Cole-Golts syndrome. Focal dermic hypoplasia. Report of a case]. Zenteno Vacheron JS, Monroy Astudillo MJ. Bol Med Hosp Infant Mex; 1975; 32(3):503-11. PubMed ID: 1138719 [Abstract] [Full Text] [Related]
42. Clinical and genetic heterogeneity in frontometaphyseal dysplasia: severe progressive scoliosis in two families. Morava E, Illés T, Weisenbach J, Kárteszi J, Kosztolányi G. Am J Med Genet A; 2003 Jan 30; 116A(3):272-7. PubMed ID: 12503106 [Abstract] [Full Text] [Related]
44. Yunis-Varon syndrome with severe osteodysplasty. Garrett C, Berry AC, Simpson RH, Hall CM. J Med Genet; 1990 Feb 30; 27(2):114-21. PubMed ID: 2319578 [Abstract] [Full Text] [Related]
46. Symphalangism and brachydactyly syndrome: report of the WL symphalangism-brachydactyly syndrome: review of literature and classification. Herrmann J. Birth Defects Orig Artic Ser; 1974 Feb 30; 10(5):23-53. PubMed ID: 4469994 [No Abstract] [Full Text] [Related]
47. Association of Wolff-Parkinson-White syndrome with congenital abnormalities of hands and feet. Niarchos AP, Finn R, Cohen HN, Buch NJ. Br Heart J; 1974 Apr 30; 36(4):409-12. PubMed ID: 4367186 [No Abstract] [Full Text] [Related]
48. Roentgenographic manifestations of the Prader-Willi syndrome. Pearson KD, Steinbach HL, Bier DM. Radiology; 1971 Aug 30; 100(2):369-77. PubMed ID: 5147402 [No Abstract] [Full Text] [Related]
49. The tricho-rhino-phalangeal syndrome. A report of 14 cases in 7 kindreds. Howell CJ, Wynne-Davies R. J Bone Joint Surg Br; 1986 Mar 30; 68(2):311-4. PubMed ID: 3958020 [Abstract] [Full Text] [Related]
50. Frontometaphyseal dysplasia with congenital urinary tract malformations. Kanemura T, Orii T, Ohtani M. Clin Genet; 1979 Dec 30; 16(6):399-404. PubMed ID: 527247 [Abstract] [Full Text] [Related]
51. A further case of opsismodysplasia with hydrocephalus. Ramos FJ, González JP, Cortabarria C, Domenech E, Pérez-González J, Bueno M. Eur J Med Genet; 2006 Dec 30; 49(1):93-100. PubMed ID: 16473316 [Abstract] [Full Text] [Related]
52. Sibs with mental retardation, supraorbital sclerosis, and metaphyseal dysplasia: frontometaphyseal dysplasia, craniometaphyseal dysplasia, or a new syndrome? Reardon W, Hall CM, Dillon MJ, Baraitser M. J Med Genet; 1991 Sep 30; 28(9):622-6. PubMed ID: 1956063 [Abstract] [Full Text] [Related]
53. [Mesomelic dysplasia: presentation of a case and literature of Werner's syndrome]. Hesselschwerdt HJ, Heisel J. Z Orthop Ihre Grenzgeb; 1990 Sep 30; 128(5):466-72. PubMed ID: 2147335 [Abstract] [Full Text] [Related]
54. Mohr syndrome in two siblings. Gencík A, Gencíkova A. J Genet Hum; 1983 Dec 30; 31(4):307-15. PubMed ID: 6663289 [Abstract] [Full Text] [Related]
55. [Pyle's metaphyseal dysplasia]. Mabille JP, Benoit JP, Castera D. Ann Radiol (Paris); 1973 Dec 30; 16(11):723-30. PubMed ID: 4779476 [No Abstract] [Full Text] [Related]
56. Esophageal atresia with distal tracheoesophageal fistula in a patient with fronto-metaphyseal dysplasia. Franceschini P, Guala A, Licata D, Franceschini D, Signorile F, Di Cara G. Am J Med Genet; 1997 Nov 28; 73(1):10-4. PubMed ID: 9375915 [Abstract] [Full Text] [Related]
57. Acrodysostosis. A syndrome of peripheral dysostosis, nasal hypoplasia, and mental retardation. Robinow M, Pfeiffer RA, Gorlin RJ, McKusick VA, Renuart AW, Johnson GF, Summitt RL. Am J Dis Child; 1971 Mar 28; 121(3):195-203. PubMed ID: 5551869 [No Abstract] [Full Text] [Related]
58. Fuhrmann syndrome associated with cortical dysplasia. Aynaci FM, Aynaci O, Ahmetoğlu A, Celep F. Genet Couns; 2001 Mar 28; 12(1):49-54. PubMed ID: 11332978 [Abstract] [Full Text] [Related]
59. Prenatal diagnosis of cloverleaf skull: watch the hands! Gorincour G, Rypens F, Grignon A, Garel L, Bortoluzzi P, Oligny L, Lemyre E, Duperron L. Fetal Diagn Ther; 2005 Mar 28; 20(4):296-300. PubMed ID: 15980644 [Abstract] [Full Text] [Related]