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Journal Abstract Search
184 related items for PubMed ID: 4282264
61. Bilateral choanal narrowing as a presentation of craniometaphyseal dysplasia. Cheung VG, Boechat MI, Barrett CT. J Perinatol; 1997; 17(3):241-3. PubMed ID: 9210083 [No Abstract] [Full Text] [Related]
62. Mucolipidosis III. Robinow M. Birth Defects Orig Artic Ser; 1974; 10(12):267-73. PubMed ID: 4282261 [No Abstract] [Full Text] [Related]
63. 3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome). Verloes A, Dresse MF, Jovanovic M, Dodinval P, Geubelle F. Clin Genet; 1989 Mar; 35(3):205-8. PubMed ID: 2650935 [Abstract] [Full Text] [Related]
64. [A new case of Stiff Skin syndrome]. Bodemer C, Habib K, Teillac D, Munich A, de Prost Y. Ann Dermatol Venereol; 1991 Mar; 118(11):805-6. PubMed ID: 1789638 [No Abstract] [Full Text] [Related]
67. Craniometaphyseal dysplasia: a case report. Thomas M, Shah MD. Indian Pediatr; 1974 Feb; 12(2):145-8. PubMed ID: 4851207 [No Abstract] [Full Text] [Related]
68. [Disease picture of congenital bowing of long bones]. Rupprecht E, Manitz U. Helv Paediatr Acta; 1973 Nov; 28(5):467-76. PubMed ID: 4773227 [No Abstract] [Full Text] [Related]
70. Restrictive dermopathy, a lethal form of arthrogryposis multiplex with skin and bone dysplasias: three new cases and review of the literature. Verloes A, Mulliez N, Gonzales M, Laloux F, Hermanns-Lê T, Piérard GE, Koulischer L. Am J Med Genet; 1992 Jun 01; 43(3):539-47. PubMed ID: 1605246 [Abstract] [Full Text] [Related]
71. A syndrome of hemimaxillary enlargement, asymmetry of the face, tooth abnormalities, and skin findings (HATS). Welsch MJ, Stein SL. Pediatr Dermatol; 2004 Jun 01; 21(4):448-51. PubMed ID: 15283787 [Abstract] [Full Text] [Related]
77. [Unusual case of hyperostosis of the type "cranio-diaphyseal dysplasia"]. Menichini G, Scarfò GB, Cantore GP, Marchetti PG, Tomaccini D. Minerva Pediatr; 1977 Jul 14; 29(23):1485-97. PubMed ID: 895688 [No Abstract] [Full Text] [Related]
78. Congenital bowing of long bones: clinical and experimental study. Nogami H, Oohira A, Kuroyanagi M, Mizutani A. Teratology; 1986 Feb 14; 33(1):1-7. PubMed ID: 3738801 [Abstract] [Full Text] [Related]
79. Frontometaphyseal Dysplasia. Evidence for dominant inheritance. Weiss L, Reynolds WA, Szymanowski RT. Am J Dis Child; 1976 Mar 14; 130(3):259-61. PubMed ID: 1258835 [Abstract] [Full Text] [Related]
80. Undiagnosed syndrome of psychomotor retardation, low birthweight dwarfism, skeletal, dental, dermal and genital anomalies. Elliott DE. Birth Defects Orig Artic Ser; 1975 Mar 14; 11(2):364-7. PubMed ID: 1241660 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]