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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2000 1
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2009 2
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33 results

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Page 1
PAPSS2 mutations cause autosomal recessive brachyolmia.
Miyake N, Elcioglu NH, Iida A, Isguven P, Dai J, Murakami N, Takamura K, Cho TJ, Kim OH, Hasegawa T, Nagai T, Ohashi H, Nishimura G, Matsumoto N, Ikegawa S. Miyake N, et al. Among authors: isguven p. J Med Genet. 2012 Aug;49(8):533-8. doi: 10.1136/jmedgenet-2012-101039. Epub 2012 Jul 11. J Med Genet. 2012. PMID: 22791835
Thyroxine hair content in congenital hypothyroidism and hyperthyroidism.
Zamboni G, Camilot M, Francia G, Lauriola S, Arslanoglu I, Isguven P, Tatò L. Zamboni G, et al. Among authors: isguven p. J Pediatr Endocrinol Metab. 2003 Mar;16(3):379-82. doi: 10.1515/jpem.2003.16.3.379. J Pediatr Endocrinol Metab. 2003. PMID: 12705362 Clinical Trial.
Atrial and ventricular arryhthmogenic potential in Turner Syndrome.
Sozen AB, Cefle K, Kudat H, Ozturk S, Oflaz H, Pamukcu B, Akkaya V, Isguven P, Palanduz S, Ozcan M, Goren T, Guven O. Sozen AB, et al. Among authors: isguven p. Pacing Clin Electrophysiol. 2008 Sep;31(9):1140-5. doi: 10.1111/j.1540-8159.2008.01154.x. Pacing Clin Electrophysiol. 2008. PMID: 18834465
33 results