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9篇 您的检索式：作者名="Elanko"

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		题名	作者	年代	出处	被引量
	1	Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosyaostosis显示文摘	Karl SH Elanko N Johnson D	2002	Am J Hum Genet2002，70，2：	1
	2	Functional haploinsufficiency of the human homeobox gene Msx2 canses defects in skull ossification 显示文摘	Wilkie AO Tang Z Elanko N	2000	Nat Genet2000，24，4：	1
	3	Genomic screening of fibroblast growth-factor receptor of 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis显示文摘	Kan SH Elanko N Johnson D		0，，：	1
	4	Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis 显示文摘	Kan SH Elanko N Johnson D	2002	Am J Hum Genet2002，70，2：	1
	5	Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification显示文摘	Wilkie AOM Tang Z Elanko N	2004	Nat Genet2004，24，：	1
	6	Functional haploinsufficiency of the human homeobox gene Msx 2 causes defects in skull ossification显示文摘	Wilkie AO Tang Z Elanko N	2000	Nat Genet2000，24，4：	1
	7	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
	8	Genomic screening of fibroblast growth factor receptor 2 reveals a wide spetrum of mutations in patients with syndromic craniosynostosis显示文摘	Kan S H Elanko N Johnson D	2002	Am J Hum Genet2002，70，：	1
	9	Genomic screening of fibroblast growth factor receptor 2 reveals a wide spectrum of mutations in patients with syndromie eraniosynostosis 显示文摘	Kan SH Elanko N Johnson D	2002	Hum Genet2002，70，：	1

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