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14篇 您的检索式：作者名="EDOUARD T"

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		题名	作者	年代	出处	被引量
	1	Expression of CONNEXIN43 is highly sensitive to ionizing radiation and other environmental stresses 显示文摘	Edouard I A Sonia M T John B L	2003	Cancer Research2003，63，21：	1
	2	Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism:identification a cryptic donor splice site in the exon 19显示文摘	Targovnik HM Edouard T Varela V		0，，01：	1
	3	Intracranial hypotension in a girl with Marfan syndrome :case report and review of the literature Childs Nerv Syst显示文摘	Cheuret E Edouard T Mejdoubi M	2008	Childs Nerv Syst2008，24，：	1
	4	Respiratory carbon fluxes in leaves 显示文摘	Guillaume T Edouard B Aline M	2012	Current Opinion in Plant Biology2012，15，3：	1
	5	Intracranial hypotension in a girl with Marfan syndrome:case report and review of the literature显示文摘	Cheuret E Edouard T Mejdoubi M	2008	Childs Nerv Syst2008，24，4：	1
	6	Ultrasonic monitoring of sol-gel transition of natural hydrocolloids显示文摘	Malika T Bertrand N Edouard R	2003	Journal of Food Engineering2003，58，1：	1
	7	Efficacy and safety of 2 - year etidronate treatment in a child with generalized arterial calcification of infancy 显示文摘	Edouard T Chabot G Miro J	2011	Eur J Pediatr2011，170，：	1
	8	Delayed puberty显示文摘	EDOUARD T TAUBER M	2010	Arch Pediatr2010，17，2：	1
	9	Functional effects of PTPN11 (SHP-2) mutations causing LEOPARD syndrome on epi- dermal growth factor-induced phosphoinositide 3-kinase/AKT/ glycogen synthase kinase 3β signaling 显示文摘	Edouard T Colnbier J P Nedelec A	2010	Mol Cell B iol2010，30，10：	1
	10	Functional effects of PTPN11 (SHP2) mutations causing LEOPARD syndrome on epidermal growth factor-induced phosphoinositide 3-kinase/AKT/glycogen synthase kinase 3显示文摘	Edouard T Combier J P N6d61ec A	2010	Molecular and Cellular Biology2010，30，10：	1
	11	Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability显示文摘	P Callier B Aral N Hanna S Lambert H Dindy C Ragon M Payet G Collod‐Beroud V Carmignac MA Delrue C Goizet N Philip T Busa Y Dulac I Missotte Y Sznajer A Toutain C Francannet A Megarbane S Julia T Edouard P Sarda J Amiel S Lyonnet V Cormier‐Daire B Gilbert	2013	Clin Genet2013，，6：	1
	12	Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature显示文摘	De Rocca Serra-N6d61ec A Edouard T Tr6guer K	2012	Proc Natl Acad Sci USA2012，109，11：	1
	13	Noonan syndrome-causing SHP2 mutants inhibit insulinlike growth factor 1 release via growth hormone-induced ERK hyperactivation,which contributes to short stature显示文摘	De Rocca Serra-Nedelec A Edouard T Treguer K	2012	Proc Natl Acad Sci USA2012，109，11：	1
	14	Relationship between vitamin D status and bone mineralization, mass, and metabolism in children with osteogenesis imperfecta: Histomorphometric study显示文摘	EDOUARD T GLORIEUX F H RAUCH F	2011	J Bone Miner Res2011，26，9：	1

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