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7. Achondroplasia-hypochondroplasia complex in a newborn infant. Huggins MJ; Smith JR; Chun K; Ray PN; Shah JK; Whelan DT Am J Med Genet; 1999 Jun; 84(5):396-400. PubMed ID: 10360392 [TBL] [Abstract][Full Text] [Related]
8. Patient with double heterozygosity for achondroplasia and pseudoachondroplasia, with comments on these conditions and the relationship between pseudoachondroplasia and multiple epiphyseal dysplasia, Fairbank type. Langer LO; Schaefer GB; Wadsworth DT Am J Med Genet; 1993 Oct; 47(5):772-81. PubMed ID: 8267011 [TBL] [Abstract][Full Text] [Related]
10. Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndrome. Nevin NC; Thomas PS; Hutchinson J Am J Med Genet; 1986 May; 24(1):33-9. PubMed ID: 3706411 [TBL] [Abstract][Full Text] [Related]
11. The roentgenographic features of homocystinuria. Morreels CL; Fletcher BD; Weilbaecher RG; Dorst JP Radiology; 1968 Jun; 90(6):1150-8. PubMed ID: 5656735 [No Abstract] [Full Text] [Related]
12. Achondroplasia and hypochondroplasia. Comments on frequency, mutation rate, and radiological features in skull and spine. Oberklaid F; Danks DM; Jensen F; Stace L; Rosshandler S J Med Genet; 1979 Apr; 16(2):140-6. PubMed ID: 458831 [TBL] [Abstract][Full Text] [Related]
13. [The pseudoachondroplastic form of spondyloepiphyseal dysplasia: apropos of 2 cases]. Cataldo F; Viani G; Albeggiani A Pediatr Med Chir; 1989; 11(3):359-63. PubMed ID: 2594570 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Hypochondroplasia: radiological diagnosis and differential diagnosis. Fasanelli S Basic Life Sci; 1988; 48():163-6. PubMed ID: 3240246 [No Abstract] [Full Text] [Related]
16. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia. Bellus GA; McIntosh I; Smith EA; Aylsworth AS; Kaitila I; Horton WA; Greenhaw GA; Hecht JT; Francomano CA Nat Genet; 1995 Jul; 10(3):357-9. PubMed ID: 7670477 [TBL] [Abstract][Full Text] [Related]
17. Hypochondroplasia: clinical and radiological aspects in 39 cases. Hall BD; Spranger J Radiology; 1979 Oct; 133(1):95-100. PubMed ID: 472320 [TBL] [Abstract][Full Text] [Related]
18. [Mutations in the Fibroblast Growth Factor Receptor 3 gene (FGFR3) in Chilean patients with idiopathic short stature, hypochondroplasia and achondroplasia]. Mancilla EE; Poggi H; Repetto G; GarcĂa C; Foradori A; Cattani A Rev Med Chil; 2003 Dec; 131(12):1405-10. PubMed ID: 15022403 [TBL] [Abstract][Full Text] [Related]
19. Dyggve-Melchiore-Clausen dysplasia (DMC): syndrome associated with a micropenis. Latrech H; Skiker I; Bentata Y; Alami Z; Mouhib Lav O; Oulali N; Benajiba N; Benmassoud S; El Jabri M; Gaouzi A; Gharbi MH; Chradibi A Pediatr Endocrinol Rev; 2013 Dec; 11(2):181-5. PubMed ID: 24575553 [TBL] [Abstract][Full Text] [Related]
20. Thanatophoric dwarfism. A condition confused with achondroplasia in the neonate, with brief comments on achondrogenesis and homozygous achondroplasia. Langer LO; Spranger JW; Greinacher I; Herdman RC Radiology; 1969 Feb; 92(2):285-94 passim. PubMed ID: 4885523 [No Abstract] [Full Text] [Related] [Next] [New Search]