These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
133 related items for PubMed ID: 3381667
1. Congenital medullary tubular stenosis. A case of Caffey-Kenny syndrome. Enriquez EJ, Toledo F, Bustamante-Cruz M, Cruz GM. Acta Orthop Scand; 1988 Jun; 59(3):326-7. PubMed ID: 3381667 [Abstract] [Full Text] [Related]
3. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant. Franceschini P, Testa A, Bogetti G, Girardo E, Guala A, Lopez-Bell G, Buzio G, Ferrario E, Piccato E. Am J Med Genet; 1992 Jan 01; 42(1):112-6. PubMed ID: 1308349 [Abstract] [Full Text] [Related]
8. Kenny-Caffey syndrome: an Arab variant? Sabry MA, Farag TI, Shaltout AA, Zaki M, Al-Mazidi Z, Abulhassan SJ, Al-Torki N, Quishawi A, Al Awadi SA. Clin Genet; 1999 Jan 15; 55(1):44-9. PubMed ID: 10066031 [Abstract] [Full Text] [Related]
9. The Lenz-Majewski hyperostotic dwarfism. A syndrome of multiple congenital anomalies, mental retardation, and progressive skeletal sclerosis. Robinow M, Johanson AJ, Smith TH. J Pediatr; 1977 Sep 15; 91(3):417-21. PubMed ID: 894410 [Abstract] [Full Text] [Related]
10. The Kenny syndrome, a rare type of growth deficiency with tubular stenosis, transient hypoparathyroidism and anomalies of refraction. Majewski F, Rosendahl W, Ranke M, Nolte K. Eur J Pediatr; 1981 Mar 15; 136(1):21-30. PubMed ID: 7215388 [Abstract] [Full Text] [Related]
11. Long-term follow up of a case of kyphomelic dysplasia. Maffulli N, Blakeway C, Fixsen JA. Orthopedics; 1993 Jan 15; 16(1):86-9. PubMed ID: 8421665 [No Abstract] [Full Text] [Related]
12. Metaphyseal and epiphyseal dysplasia with unusual facies and cataract. Kozlowski K, Rafinski T, Kucharska K. Am J Dis Child; 1973 Apr 15; 125(4):553-6. PubMed ID: 4699894 [No Abstract] [Full Text] [Related]
13. [Kenny-Caffey syndrome and its related syndromes]. Isojima T, Kitanaka S. Nihon Rinsho; 2015 Nov 15; 73(11):1959-64. PubMed ID: 26619675 [Abstract] [Full Text] [Related]
14. The radiologic assessment of short stature--dwarfism. Dorst JP, Scott CI, Hall JG. Radiol Clin North Am; 1972 Aug 15; 10(2):393-414. PubMed ID: 4262226 [No Abstract] [Full Text] [Related]
15. Kenny-Caffey syndrome. Case report and literature review. Abdel-Al YK, Auger LT, el-Gharbawy F. Clin Pediatr (Phila); 1989 Apr 15; 28(4):175-9. PubMed ID: 2649298 [Abstract] [Full Text] [Related]
17. [Clinical and genetic heterogeneity in Robinow's syndrome. Report of a new case and review of the literature I]. Oliván Gonzalvo G, Pérez González JM, Ventura Faci P, Olivares López JL, Bueno Sánchez M. An Esp Pediatr; 1990 Jul 15; 33(1):76-81. PubMed ID: 2252296 [No Abstract] [Full Text] [Related]
19. Radiological case of the month. Dyschondrosteosis (Leri-Weill Syndrome). Gwinn JL, Lee FA. Am J Dis Child; 1972 Aug 15; 124(2):243-4. PubMed ID: 5052409 [No Abstract] [Full Text] [Related]