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24. Association of achondroplasia with Down syndrome: difficulty in prenatal diagnosis by sonographic and 3-D helical computed tomographic analyses. Kaga A; Murotsuki J; Kamimura M; Kimura M; Saito-Hakoda A; Kanno J; Hoshi K; Kure S; Fujiwara I Congenit Anom (Kyoto); 2015 May; 55(2):116-20. PubMed ID: 25385298 [TBL] [Abstract][Full Text] [Related]
25. Failure to early prenatal diagnosis in classic achondroplasia. Hall JG; Golbus MS; Graham CB; Pagon RA; Luthy DA; Filly RA Am J Med Genet; 1979; 3(4):371-5. PubMed ID: 474637 [No Abstract] [Full Text] [Related]
26. [Prenatal ultrasonic diagnosis of skeletal malformations]. Cecuk S; Polak J; Plesa M; Jukić S; Gorski V Jugosl Ginekol Opstet; 1983; 23(5-6):136-40. PubMed ID: 6679004 [TBL] [Abstract][Full Text] [Related]
27. [Homozygous form of achondroplasia and thanatophoric dwarfism--bone dysplasias to be diagnosed before birth]. Rogovits N; Weissenbacher G; Zweymüller E Geburtshilfe Frauenheilkd; 1972 Mar; 32(3):184-91. PubMed ID: 5063577 [No Abstract] [Full Text] [Related]
28. Low bone mineral density in achondroplasia and hypochondroplasia. Matsushita M; Kitoh H; Mishima K; Kadono I; Sugiura H; Hasegawa S; Nishida Y; Ishiguro N Pediatr Int; 2016 Aug; 58(8):705-8. PubMed ID: 26716907 [TBL] [Abstract][Full Text] [Related]
30. Ultrasound and molecular mid-trimester prenatal diagnosis of de novo achondroplasia. Mesoraca A; Pilu G; Perolo A; Novelli G; Salfi N; Lucchi A; Bovicelli L; Dallapiccola B Prenat Diagn; 1996 Aug; 16(8):764-8. PubMed ID: 8878289 [TBL] [Abstract][Full Text] [Related]
31. [Sonographic diagnosis of a case of type 1 achondrogenesis in the 2d trimester]. Schramm T; Nerlich A Geburtshilfe Frauenheilkd; 1989 Oct; 49(10):917-9. PubMed ID: 2684730 [TBL] [Abstract][Full Text] [Related]
32. [Hypochondroplasia: importance of radiological findings in the differential diagnosis of short statures of different origin]. Iannaccone R; Tiberti AC Recenti Prog Med; 2001; 92(7-8):483-8. PubMed ID: 11475794 [TBL] [Abstract][Full Text] [Related]
33. Prenatal DNA diagnosis of a single-gene disorder from maternal plasma. Saito H; Sekizawa A; Morimoto T; Suzuki M; Yanaihara T Lancet; 2000 Sep; 356(9236):1170. PubMed ID: 11030304 [TBL] [Abstract][Full Text] [Related]
34. [Rapid genetic prenatal diagnosis for achondroplasia]. Zhu HY; Yang Y; Li J; Ru T; Hu YL Zhonghua Fu Chan Ke Za Zhi; 2008 Nov; 43(11):810-3. PubMed ID: 19087561 [TBL] [Abstract][Full Text] [Related]
35. In utero diagnosis of achondrogenesis, type I. Smith WL; Breitweiser TD; Dinno N Clin Genet; 1981 Jan; 19(1):51-4. PubMed ID: 7460382 [No Abstract] [Full Text] [Related]