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Journal Abstract Search
152 related items for PubMed ID: 7447519
1. [The lesions associated with leprechaunism (author's transl)]. Lebreuil G, Pizzi M, Sebaoun M, Oddou JH. Arch Anat Cytol Pathol; 1980; 28(5):310-6. PubMed ID: 7447519 [No Abstract] [Full Text] [Related]
2. Leprechaunism (Donohue's syndrome): a case report. Tokatli A, Ozsoylu S, Ozme S. Turk J Pediatr; 1993; 35(4):319-22. PubMed ID: 8160285 [Abstract] [Full Text] [Related]
3. Leprechaunism in two Turkish patients. Gürgey A, Göğüş S, Saatçi U, Bilginturan N, Yordam N, Coşkun T, Ozkutlu S, Sahin N. Turk J Pediatr; 1997; 39(3):387-93. PubMed ID: 9339119 [Abstract] [Full Text] [Related]
4. Larsen syndrome in siblings with consanguineous parents. Topley JM, Varady E, Lestringant GG. Clin Dysmorphol; 1994 Jul; 3(3):263-5. PubMed ID: 7526939 [Abstract] [Full Text] [Related]
12. Geleophysic dysplasia. Wraith JE, Bankier A, Chow CW, Danks DM, Sardharwalla IB. Am J Med Genet; 1990 Feb; 35(2):153-6. PubMed ID: 2090119 [Abstract] [Full Text] [Related]
13. Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome. Maróti Z, Kutsche K, Sutajova M, Gal A, Nothwang HG, Czeizel AE, Tímár L, Sólyom E. Am J Med Genet; 2002 May 01; 109(3):234-7. PubMed ID: 11977185 [No Abstract] [Full Text] [Related]
15. [Larsen's syndrome, inborn articular and osseous dysplasia connected with a characteristic face (author's transl)]. Fait M, Janovec M. Acta Chir Orthop Traumatol Cech; 1975 Feb 01; 42(1):19-32. PubMed ID: 1119288 [No Abstract] [Full Text] [Related]
16. Kabuki syndrome: report of six Thai children and further phenotypic and genetic delineation. Shotelersuk V, Punyashthiti R, Srivuthana S, Wacharasindhu S. Am J Med Genet; 2002 Jul 15; 110(4):384-90. PubMed ID: 12116214 [Abstract] [Full Text] [Related]
18. [Larsen syndrome and idiopathic hypercalciuria]. Tardio Torio E, Sánchez Sánchez E, Pérez Prado C. An Esp Pediatr; 1993 Nov 15; 39(5):467-9. PubMed ID: 8285473 [No Abstract] [Full Text] [Related]
19. Growth deficiency, facial dysmorphogenesis and brachydactyly: a new syndrome. Frias JL, Guttery EG, Felman AH. Birth Defects Orig Artic Ser; 1975 Nov 15; 11(2):30-3. PubMed ID: 1227535 [No Abstract] [Full Text] [Related]
20. Long-term evaluation of a child with the branchio-oculo-facial syndrome. Schmerler S, Kushnick T, Desposito F. Am J Med Genet; 1992 Sep 15; 44(2):177-8. PubMed ID: 1456287 [Abstract] [Full Text] [Related] Page: [Next] [New Search]