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24篇 您的检索式：作者名="Cogan JD"

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	题名	作者	年代	出处	被引量
1	The PROP12-base pair deletion is a common cause of combined pituitary hormone deficiency显示文摘	Cogan JD Wu W Phillips JA 3rd	1998	J Clin Endocrinol Metab1998，83，：	1
2	Telomerase mutationsin families with idiopathic pulmonary fibrosis显示文摘	Armanios MY Chen JJ Cogan JD	2007	N Engl J Med2007，356，13：	1
3	Gross BMPR2 gene rearrangements constitute a new cause for primarypulmonary hypertension 显示文摘	Cogan JD Vnencak-Jones C Pratrap S	2005	Genet Med2005，7，3：	1
4	Telomerase mutations in families with idiopathic pulmonary fibrosis显示文摘	Armanios MY Chen JJ Cogan JD		0，，：	1
5	Mutations in PROPIcause familial combined pituitary hormone deficiency显示文摘	Wu W Cogan JD Pfaffle RW	1998	Nat Genet1998，18，：	1
6	Alterations in oestrogen metabolism : implications for higher penetrance of familial pulmonary arterial hypertension in females 显示文摘	Austin ED Cogan JD West JD	2009	Eur Respir J2009，34，：	1
7	Familial growth hormone deficiency:a model of dominant and recessive mutations affecting a monomeric protein显示文摘	Cogan JD Phillips JA Schenkman SS	1994	J Clin Endocrinal Metab1994，79，5：	1
8	Allelic variations in the human growth hormone-1 gene promoter of growth hormone deficient patients and normal controls显示文摘	Wagner JK Eble A Cogan JD	1997	Enr J Endocrinol1997，137，5：	1
9	Telomerase mutations in families with idiopathic pulmonary fibrosis 显示文摘	Armanios MY Chen JJ Cogan JD	2007	N Engl J Med2007，356，13：	1
10	Telomerase mutations in families with idiopathic pulmonary fibrosis显示文摘	Armanios MY Chen JJ Cogan JD	2007	N Engl J Med2007，356，：	1
11	High frequency of BMPR2 exonie deletions/duplications in familial pulmonary arterial hypertension显示文摘	Cogan JD Paueiulo MW Batehman AP	2006	Am J Respir Crit Care Med2006，174，5：	1
12	Photodiode circuits for retinal prostheses显示文摘	Loudin JD Cogan SF Mathieson K	2011	IEEE Trans Biomed Circuits Syst2011，5，5：	1
13	Telomerase mutations infamilies with idiopathic pulmonary fibrosis 显示文摘	Armanios MY Chen JJ Cogan JD etal	2007	N Engl J Med2007，356，13：	1
14	Mutations in PROP1 cause familial combined pituitary hormone deficiency 显示文摘	Wu W Cogan JD Pfaffle RW	1998	Nat Genet1998，18，：	1
15	Telomerase mutations in families with idiopathic pulmonary fibrosis显示文摘	Armanios MY Chen JJ Cogan JD		0，，13：	1
16	Telomerase mutations in families with idiopathic pulmonary fibrosis 显示文摘	Armanios MY Chen JJ Cogan JD	2007	N Engl J Med2007，356，13：	1
17	Heterogeneous growth (GH) gene mutations in familial GH deficiency显示文摘	Cogan JD Phillips Ⅲ JA Sakati N	1993	J Clin Endocrinol Metab1993，76，：	1
18	Telomerase mutations in families with idiopathic pulmonary fibrosis显示文摘	Armnios MY Chen JJ Cogan JD		0，，：	1
19	Telomerase mutations in families with idiopathic pulmonary fibrosis显示文摘	Armanios MY Chen JJ Cogan JD	2007	N Engl J Med2007，356，13：	1
20	Heterogeneous growth hormone(GH) gene mutations in familial GH deficiency显示文摘	Cogan JD Phillips JA Sakati N	1993	J Clin Endocrinol Metab1993，76，：	1

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