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24. Compound heterozygosity for the Achondroplasia-hypochondroplasia FGFR3 mutations: prenatal diagnosis and postnatal outcome. Chitayat D; Fernandez B; Gardner A; Moore L; Glance P; Dunn M; Chun K; Sgro M; Ray P; Allingham-Hawkins D Am J Med Genet; 1999 Jun; 84(5):401-5. PubMed ID: 10360393 [TBL] [Abstract][Full Text] [Related]
25. Prenatal ultrasound and MRI findings of temporal and occipital lobe dysplasia in a twin with achondroplasia. Pugash D; Lehman AM; Langlois S Ultrasound Obstet Gynecol; 2014 Sep; 44(3):365-8. PubMed ID: 24616001 [TBL] [Abstract][Full Text] [Related]
26. Multiplex PCR in noninvasive prenatal diagnosis for FGFR3-related disorders. Terasawa S; Kato A; Nishizawa H; Kato T; Yoshizawa H; Noda Y; Miyazaki J; Ito M; Sekiya T; Fujii T; Kurahashi H Congenit Anom (Kyoto); 2019 Jan; 59(1):4-10. PubMed ID: 29542187 [TBL] [Abstract][Full Text] [Related]
27. Successful obstetric and anaesthetic management of a pregnant woman with achondroplasia. Melekoglu R; Celik E; Eraslan S BMJ Case Rep; 2017 Oct; 2017():. PubMed ID: 29070618 [TBL] [Abstract][Full Text] [Related]
28. [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]
29. Australian guidelines for the management of children with achondroplasia. Tofts LJ; Armstrong JA; Broley S; Carroll T; Ireland PJ; Koo M; Langdon K; McGregor L; McKenzie F; Mehta D; Savarirayan R; Tate T; Wesley A; Zankl A; Jenner M; Eyles M; Pacey V J Paediatr Child Health; 2023 Feb; 59(2):229-241. PubMed ID: 36628540 [TBL] [Abstract][Full Text] [Related]
30. In utero analysis of heterozygous achondroplasia: variable time of onset as detected by femur length measurements. Kurtz AB; Filly RA; Wapner RJ; Golbus MS; Rifkin MR; Callen PW; Pasto ME J Ultrasound Med; 1986 Mar; 5(3):137-40. PubMed ID: 3517360 [TBL] [Abstract][Full Text] [Related]
31. [Achondroplasia revealed by ultrasound in utero]. Mladinov G; Krzisnik Z Jugosl Ginekol Opstet; 1977; 17(4):239-41. PubMed ID: 616497 [No Abstract] [Full Text] [Related]
32. Achondroplasia with 47, XXY karyotype: a case report of the neonatal diagnosis of an extremely unusual association. Ros-Pérez P; Regidor FJ; Colino E; Martínez-Payo C; Barroso E; Heath KE BMC Pediatr; 2012 Jun; 12():88. PubMed ID: 22747519 [TBL] [Abstract][Full Text] [Related]
33. Living with achondroplasia: attitudes toward population screening and correlation with quality of life. Gollust SE; Thompson RE; Gooding HC; Biesecker BB Prenat Diagn; 2003 Dec; 23(12):1003-8. PubMed ID: 14663838 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. Antenatal diagnosis of achondrogenesis type II. Kodandapani S; Ramkumar V JNMA J Nepal Med Assoc; 2009; 48(174):155-7. PubMed ID: 20387359 [TBL] [Abstract][Full Text] [Related]
37. [Fetal achondroplasia--antenatal diagnosis of two cases]. Nikolov A; Markov D; Nashar S Akush Ginekol (Sofiia); 2008; 47(4):40-3. PubMed ID: 19227764 [TBL] [Abstract][Full Text] [Related]
38. [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]
40. [Prenatal diagnose of abnormalities of fetal limb bone]. Song J; Wang X Zhonghua Fu Chan Ke Za Zhi; 2010 Oct; 45(10):745-9. PubMed ID: 21176554 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]