208 related articles for article (PubMed ID: 11101832)
1. Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation.
Thompson AA; Nguyen LT
Nat Genet; 2000 Dec; 26(4):397-8. PubMed ID: 11101832
[No Abstract] [Full Text] [Related]
2. HOXA11 mutation in amegakaryocytic thrombocytopenia with radio-ulnar synostosis syndrome inhibits megakaryocytic differentiation in vitro.
Horvat-Switzer RD; Thompson AA
Blood Cells Mol Dis; 2006; 37(1):55-63. PubMed ID: 16765069
[TBL] [Abstract][Full Text] [Related]
3. Proximal radio-ulnar synostosis with bone marrow failure syndrome in an infant without a HOXA11 mutation.
Castillo-Caro P; Dhanraj S; Haut P; Robertson K; Dror Y; Sharathkumar AA
J Pediatr Hematol Oncol; 2010 Aug; 32(6):479-85. PubMed ID: 20562651
[TBL] [Abstract][Full Text] [Related]
4. Congenital thrombocytopenia and radio-ulnar synostosis: a new familial syndrome.
Thompson AA; Woodruff K; Feig SA; Nguyen LT; Schanen NC
Br J Haematol; 2001 Jun; 113(4):866-70. PubMed ID: 11442476
[TBL] [Abstract][Full Text] [Related]
5. A neonate with severe thrombocytopenia and radio-ulnar synostosis.
Sola MC; Slayton WB; Rimsza LM; Perez JA; Fuchs D; Calhoun DA; Christensen RD
J Perinatol; 2004 Aug; 24(8):528-30. PubMed ID: 15282617
[TBL] [Abstract][Full Text] [Related]
6. Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia.
Niihori T; Ouchi-Uchiyama M; Sasahara Y; Kaneko T; Hashii Y; Irie M; Sato A; Saito-Nanjo Y; Funayama R; Nagashima T; Inoue S; Nakayama K; Ozono K; Kure S; Matsubara Y; Imaizumi M; Aoki Y
Am J Hum Genet; 2015 Dec; 97(6):848-54. PubMed ID: 26581901
[TBL] [Abstract][Full Text] [Related]
7. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
Giuffrè L; Corsello G; Giuffrè M; Piccione M; Albanese A
Am J Med Genet; 1994 Jul; 51(3):266-9. PubMed ID: 8074157
[TBL] [Abstract][Full Text] [Related]
8. A novel mutation in the MECOM gene causing radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT-2) in an infant.
Loganathan A; Munirathnam D; Ravikumar T
Pediatr Blood Cancer; 2019 Apr; 66(4):e27574. PubMed ID: 30536840
[No Abstract] [Full Text] [Related]
9. Unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance in sibs: a new syndrome.
Der Kaloustian VM; McIntosh N; Silver K; Blaichman S; Halal F
Am J Med Genet; 1992 Aug; 43(6):942-5. PubMed ID: 1384331
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Novel mutations in a child with congenital amegakaryocytic thrombocytopenia.
Pemberton LC; Levett D; Skinner R; Hall AG; Hanley JP
Br J Haematol; 2006 Dec; 135(5):742-3. PubMed ID: 17054430
[No Abstract] [Full Text] [Related]
12. [Clinico-radiological study of congenital radio ulnar synostosis].
Luna E; Nannini G
Chir Ital; 1981 Apr; 33(2):626-34. PubMed ID: 7285263
[No Abstract] [Full Text] [Related]
13. 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]
14. A case with bilateral radio-ulnar synostosis.
Koç A; Kaymak AO; Karaer K; Ergün MA; Aksu T; Perçin EF
Genet Couns; 2008; 19(2):193-8. PubMed ID: 18618994
[TBL] [Abstract][Full Text] [Related]
15. Congenital amegakaryocytic thrombocytopenia in three siblings: molecular analysis of atypical clinical presentation.
Gandhi MJ; Pendergrass TW; Cummings CC; Ihara K; Blau CA; Drachman JG
Exp Hematol; 2005 Oct; 33(10):1215-21. PubMed ID: 16219544
[TBL] [Abstract][Full Text] [Related]
16. A critical review of the surgical treatment of congenital proximal radio-ulnar synostosis.
Dal Monte A; Andrisano A; Mignani G; Bungaro P
Ital J Orthop Traumatol; 1987 Jun; 13(2):181-6. PubMed ID: 3451916
[TBL] [Abstract][Full Text] [Related]
17. Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?
Delooz J; Moerman P; Van den Berghe K; Fryns JP
Genet Couns; 1992; 3(2):91-3. PubMed ID: 1642816
[TBL] [Abstract][Full Text] [Related]
18. [On 2 cases of congenital radio-ulnar synostosis].
Colombini E; Ugolotti G
Ann Radiol Diagn (Bologna); 1969 Feb; 42(1):3-12. PubMed ID: 5406590
[No Abstract] [Full Text] [Related]
19. [Congenital radio-ulnar synostosis].
Rodríguez García L; Armendáriz Mekjavich M; Urzainki Martínez F; Otero Arévalo E; García Mata S
An Esp Pediatr; 2002 Jan; 56(1):75-6. PubMed ID: 11792254
[No Abstract] [Full Text] [Related]
20. Humero-radial synostosis with ulnar defects in sibs.
Ramer JC; Ladda RL
Am J Med Genet; 1989 Jun; 33(2):176-9. PubMed ID: 2669480
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
