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11篇 您的检索式：作者名="Tuysuz B"

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		题名	作者	年代	出处	被引量
	1	Novel NTRK1mutations cause hereditary sensory and autonomic neuropathy type IV:demonstration of a founder mutation in the Turkish population显示文摘	Tuysuz B Bayrakli F Di Luna ML	2008	Neurogenetics2008，9，：	1
	2	Clinical variability of as- phyxiating thoracic dystropHy (Jeune) syndrome: evaluation and classification of 13 patients显示文摘	Tuysuz B Baris S Aksoy F	2009	Am J Med Genet A2009，149，8：	1
	3	Mutations in the prostaglandin transporter encoding gene SLCO2A1 cause pri- mary hypertrophic osteoarthropathy and isolated digital club- bing 显示文摘	Seifert W Kuhnisch J Tuysuz B	2012	Hum Mutat2012，33，：	1
	4	Development of a passive VHF radar system using software defined radio for equatorial plasma instability studies显示文摘	Tuysuz B Urbina J and Lind F D	2013	Radio Science2013，48，4：	1
	5	Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2 显示文摘	Afzal AR Rajab A Fenske CD Oldridge M Elanko N Ternes-Pereira E Tuysuz B Murday VA Patton MA Wilkie AO Jeffery S	2000	Nat Genet2000，25，4：	1
	6	Osteoporosis-pseudoglioma syndrome: three novel mutations in the LRP5 gene and response to bisphosphonate treatment 显示文摘	Tuysuz B Bursali A Alp Z	2012	Horm Res Paediatr2012，77，2：	1
	7	Osteoporosis-pseudoglioma syndrome: three novel mutations in the LRP5 gene and response to bisphosphonate treatment 显示文摘	TuysUz B Bursal A Alp Z	2012	Horm Res Paediatr2012，77，2：	1
	8	Development of a passive VHF radar system using software-defined radio for equatorial plasma instability studies 显示文摘	TUYSUZ B URBINA J LIND D	2013	Radio science2013，48，4：	1
	9	Omani-type spondy loepiphy seal dysplasia with cardiac involvement caused by a missense mutation in CHST3显示文摘	Tuysuz B Mizumoto S Sugahara K	2009	Clin Genet2009，75，4：	1
	10	Calcitonin treatment in osteoectasia with hyper-phosphatasi(juvenile Paget's diaease):Radiographic change after treatment显示文摘	Tuysuz B Mercimek S Ungur S	1999	Pediatr Radiol1999，29，：	1
	11	Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q; 9p translocation显示文摘	Tuysuz B Demirel A Uysal S	2008	Genet Couns2008，19，1：	1

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