Zespół małopłytkowości i aplazji kości promieniowej (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Zespół małopłytkowości i aplazji kości promieniowej" in Polish language version.

refsWebsite

Global rank Polish rank

4^th place

7^th place

3,595^th place

1,361^st place

emedicine.com

Wu, JK, Wong, MP: Thrombocytopenia-Absent Radius Syndrome. eMedicine Pediatrics, 2006. [dostęp 2007-09-15]. (ang.).

Gross H, Groh C, Weippl G. Congenital hypoplastic thrombopenia with aplasia of the radius, a syndrome of multiple variations. „Neue Osterr Z kinderheilkd”. 1, s. 574-82, 1956. PMID: 13418935.
Klopocki E, Schulze H, Strauss G, Ott CE, Hall J, Trotier F, Fleischhauer S, Greenhalgh L, Newbury-Ecob RA, Neumann LM, Habenicht R, König R, Seemanova E, Megarbane A, Ropers HH, Ullmann R, Horn D, Mundlos S. Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome. „Am J Hum Genet”. 80, s. 232-240, 2007. PMID: 17236129.
Ahmad, R. A rare association of crossed fused renal ectopia. „BMC Nephrol”. 8. 5, 2007. PMID: 17331255.
Bradshaw A, Donnelly LF, Foreman JW. Thrombocytopenia and absent radii syndrome associated with horseshoe kidney. „Pediatr Nephrol”. 14, s. 29-31, 2000. PMID: 10654326.
Fivush B, Mc Grath S, Zinkham W. Thrombocytopenia absent radii syndrome associated with renal insufficiency. „Clin Pediatr (Phila)”. 29, s. 182-184, 1990. PMID: 2407410.
Strippoli P, Savoia A, Iolascon A, Tonelli R, Savino M, Giordano P, D'Avanzo M, Massolo F, Locatelli F, Borgna C, De Mattia D, Zelante L, Paolucci G, Bagnara GP. Mutational screening of thrombopoietin receptor gene (c-mpl) in patients with congenital thrombocytopenia and absent radii (TAR). „Brit J Haemat”. 103, s. 311-314, 1998. PMID: 9827898.

Klopocki E, Schulze H, Strauss G, Ott CE, Hall J, Trotier F, Fleischhauer S, Greenhalgh L, Newbury-Ecob RA, Neumann LM, Habenicht R, König R, Seemanova E, Megarbane A, Ropers HH, Ullmann R, Horn D, Mundlos S. Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome. „Am J Hum Genet”. 80, s. 232-240, 2007. PMID: 17236129.