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.
114 related articles for article (PubMed ID: 5304440)
1. [Certain mechanisms of genetic transmission in the field of osteochondro-embryopathies (Case reports)]. Ravetto F; Crua G Minerva Pediatr; 1967 Nov; 19(46):2035-41. PubMed ID: 5304440 [No Abstract] [Full Text] [Related]
2. [Rhizomelic type of chondrodysplasia punctata in 2 sisters. Evidence for hereditary transmission of a recessive autosomic type]. Fabris C; Licata D; Martano C; Silengo M; Franceschini P Minerva Pediatr; 1981 Jan; 33(2):81-5. PubMed ID: 7242481 [No Abstract] [Full Text] [Related]
5. [Orthopedic treatment of children with dysplastic diseases of the skeleton]. Wolkow MW; Andrianow WL Beitr Orthop Traumatol; 1968; 15(11):649-52. PubMed ID: 4979255 [No Abstract] [Full Text] [Related]
6. Maxillonasal dysplasia (Binder's syndrome) and chondrodysplasia punctata. Serville F J Med Genet; 1992 Feb; 29(2):141. PubMed ID: 1613767 [No Abstract] [Full Text] [Related]
7. [A combination of multiple cartilaginous exostoses and enchondromatosis of bone in a family]. Tschernikoff Z; Ditscheva L Radiol Diagn (Berl); 1989; 30(1):53-6. PubMed ID: 2785276 [TBL] [Abstract][Full Text] [Related]
8. Metachondromatosis. Report of four cases. Bassett GS; Cowell HR J Bone Joint Surg Am; 1985 Jun; 67(5):811-4. PubMed ID: 3873457 [No Abstract] [Full Text] [Related]
10. Multiple exostotic hypochondroplasia: syndrome of combined hypochondroplasia and multiple exostoses. Dominguez R; Young LW; Steele MW; Girdany BR Pediatr Radiol; 1984; 14(5):356-9. PubMed ID: 6332296 [TBL] [Abstract][Full Text] [Related]
11. Genetic skeletal dysplasias in the Museum of Pathological Anatomy, Vienna. Beighton P; Sujansky E; Patzak B; Portele KA Am J Med Genet; 1993 Nov; 47(6):843-7. PubMed ID: 8279481 [TBL] [Abstract][Full Text] [Related]
12. [The disease of multiple exostoses. Correlations with other chondrodysplasias]. Lazzari E; Vertova F Boll Soc Med Chir Cremona; 1968; 22(3):123-33. PubMed ID: 5306067 [No Abstract] [Full Text] [Related]
13. Familial and hereditary anomalies producing brachydactylia of hands: roentgen manifestations. Kellam DA J Am Osteopath Assoc; 1970 Sep; 70(1):78-100. PubMed ID: 4990165 [No Abstract] [Full Text] [Related]
14. Disorders of post-squalene cholesterol biosynthesis leading to human dysmorphogenesis. Andersson HC Cell Mol Biol (Noisy-le-grand); 2002 Mar; 48(2):173-7. PubMed ID: 11990452 [TBL] [Abstract][Full Text] [Related]
16. Stüve-Wiedemann syndrome and related bent bone dysplasias. Akawi NA; Ali BR; Al-Gazali L Clin Genet; 2012 Jul; 82(1):12-21. PubMed ID: 22300393 [TBL] [Abstract][Full Text] [Related]
17. [Hereditary exostoses--presentation of a family case]. Hayes TB; Ramstad K; Nielsen EW Tidsskr Nor Laegeforen; 1998 Oct; 118(24):3769-72. PubMed ID: 9816946 [TBL] [Abstract][Full Text] [Related]
18. Provisionally unique autosomal recessive chondrodysplasia punctata syndrome. Toriello HV; Higgins JV; Miller T Am J Med Genet; 1993 Oct; 47(5):797-9. PubMed ID: 8267015 [TBL] [Abstract][Full Text] [Related]
19. "Snail-like pelvis" chondrodysplasia: a further case report. Camera G; Scarano G; Tronci A; La Cava G; Mastroiacovo P Am J Med Genet; 1991 Sep; 40(4):513-4. PubMed ID: 1746621 [TBL] [Abstract][Full Text] [Related]
20. Genetic skeletal dysplasia in Thailand: the Siriraj experience. Wasant P; Waeteekul S; Rimoin DL; Lachman RS Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():59-67. PubMed ID: 8629144 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]