166 related articles for article (PubMed ID: 8500258)
21. Nager acrofacial dysostosis: management of a difficult airway.
Friedman RA; Wood E; Pransky SM; Seid AB; Kearns DB
Int J Pediatr Otorhinolaryngol; 1996 Mar; 35(1):69-72. PubMed ID: 8882111
[TBL] [Abstract][Full Text] [Related]
22. [Morphology and systematic aspects of the longitudinal radial defect].
Martini AK
Handchir Mikrochir Plast Chir; 1992 Jan; 24(1):16-22. PubMed ID: 1568670
[TBL] [Abstract][Full Text] [Related]
23. Deletion of 1q in a patient with acrofacial dysostosis.
Waggoner DJ; Ciske DJ; Dowton SB; Watson MS
Am J Med Genet; 1999 Feb; 82(4):301-4. PubMed ID: 10051162
[TBL] [Abstract][Full Text] [Related]
24. [Familial congenital radio-ulnar synostosis (author's transl)].
Walter E
Rofo; 1978 Aug; 129(2):241-5. PubMed ID: 151025
[TBL] [Abstract][Full Text] [Related]
25. [Distal symphalangia with humeroradial synostosis, carpal synostosis and brachyphalangia of the thumb. A dominant syndrome (author's transl)].
Lenz W; Rehmann I
Z Orthop Ihre Grenzgeb; 1976 Apr; 114(2):202-11. PubMed ID: 1274395
[TBL] [Abstract][Full Text] [Related]
26. Antley-Bixler syndrome with radioulnar synostosis.
Hurley ME; White MJ; Green AJ; Kelleher J
Pediatr Radiol; 2004 Feb; 34(2):148-51. PubMed ID: 14513299
[TBL] [Abstract][Full Text] [Related]
27. A new autosomal dominant acrofacial dysostosis syndrome.
Reynolds JF; Webb MJ; Opitz JM
Am J Med Genet Suppl; 1986; 2():143-50. PubMed ID: 3146284
[TBL] [Abstract][Full Text] [Related]
28. Familial occurrence of hemifacial microsomia with radial limb defects.
Moeschler J; Clarren SK
Am J Med Genet; 1982 Aug; 12(4):371-5. PubMed ID: 7124792
[No Abstract] [Full Text] [Related]
29. [Nager's acrofacial dysostosis (nager-de Reynier's acrofacial dysostosis syndrome). A hereditary mandibulofacial dysostosis with hypoplasia, of the extremities, especially of the thumb].
Wiedemann HR; Dibbern H
Med Welt; 1982 Jul; 33(29-30):1052-3. PubMed ID: 7121237
[No Abstract] [Full Text] [Related]
30. Congenital proximal radio-ulnar synostosis: clinical and anatomical features.
Dal Monte A; Andrisano A; Bungaro P; Mignani G
Ital J Orthop Traumatol; 1987 Jun; 13(2):201-6. PubMed ID: 3451918
[TBL] [Abstract][Full Text] [Related]
31. Expanding the phenotypic and genetic spectrum of radioulnar synostosis associated hematological disease.
Walne A; Tummala H; Ellison A; Cardoso S; Sidhu J; Sciuccati G; Vulliamy T; Dokal I
Haematologica; 2018 Jul; 103(7):e284-e287. PubMed ID: 29519864
[No Abstract] [Full Text] [Related]
32. [Variants of radial hemimelia with and without vitium cordis (Holt-Oram syndrome) in 2 families].
Pfeiffer RA; Böwing B; Deeg KH
Monatsschr Kinderheilkd; 1989 May; 137(5):275-9. PubMed ID: 2739665
[TBL] [Abstract][Full Text] [Related]
33. Otologic and audiologic features of Nager acrofacial dysostosis.
Herrmann BW; Karzon R; Molter DW
Int J Pediatr Otorhinolaryngol; 2005 Aug; 69(8):1053-9. PubMed ID: 16005346
[TBL] [Abstract][Full Text] [Related]
34. Autosomal dominant inheritance of adducted thumbs and other digital anomalies.
Miranda A; Zenteno JC; Santiago E; Kofman-Alfaro S
Clin Genet; 1998 Jul; 54(1):83-5. PubMed ID: 9727747
[TBL] [Abstract][Full Text] [Related]
35. Nager's acrofacial dysostosis with thumb duplication: report of a case.
Giugliani R; Pereira CH
Clin Genet; 1984 Sep; 26(3):228-30. PubMed ID: 6478644
[No Abstract] [Full Text] [Related]
36. Radio-ulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation.
Tsukahara M; Matsuo K; Furukawa S
Am J Med Genet; 1995 Aug; 58(2):159-60. PubMed ID: 8533809
[TBL] [Abstract][Full Text] [Related]
37. Absent tibiae, triphalangeal thumbs and polydactyly: description of a family and prenatal diagnosis.
Canún S; Lomelí RM; Martínez R; Carnevale A
Clin Genet; 1984 Feb; 25(2):182-6. PubMed ID: 6705252
[TBL] [Abstract][Full Text] [Related]
38. Nager acrofacial dysostosis and preaxial polydactyly: a further example with lethal outcome.
Petit P; Moerman P; Fryns JP
Genet Couns; 1993; 4(2):135-7. PubMed ID: 8357565
[TBL] [Abstract][Full Text] [Related]
39. Radio-ulnar synostosis in Williams syndrome. A frequently associated anomaly.
Charvat KA; Hornstein L; Oestreich AE
Pediatr Radiol; 1991; 21(7):508-10. PubMed ID: 1771116
[TBL] [Abstract][Full Text] [Related]
40. Mandibulofacial dysostosis, microtia, and limb anomalies in a newborn: a new form of acrofacial dysostosis syndrome?
Zhang Y; Dai Y; Liu Y; Ren J
Clin Genet; 2010 Dec; 78(6):570-4. PubMed ID: 20412112
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
