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27篇 您的检索式：作者名="NETCHINE I"

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	题名	作者	年代	出处	被引量
1	Pituitary stalk interruption syndrome:a clinical-biological-genetic assessment of its pathogenesis显示文摘	Pinto G Netchine I Sobrier ML	1997	J Clin Endocrinol Metab1997，82，10：	1
2	Pituitary stalk interruption syndrome:a clinical-biological-genetic assessment of its pathogenesis显示文摘	Pinto G Netchine I Sobrier ML	1997	J Clin Endocrinol Metab1997，82，10：	1
3	Beckwith- Wiedemann and Russell - Silver syndromes: from new molecular insights to the comprehension of imprinting regulation显示文摘	AZZI S ABI H W NETCHINE I	2014	Curr Opin Endocrinol Diabetes Obes2014，21，1：	1
4	Pituitary stalk inter- ruption syndrome a clinical -biological-genetic assessment of its pathogenesis 显示文摘	Pinto G Netchine I Sobrier M L	1997	Clin Endocrinol Metab1997，82，10：	1
5	Pituitary stalk interruption syndrome : a clinical-biological-genetic assessment of its pathogenesis 显示文摘	Pinto G Netchine I Sobrier ML	1997	Clin Endocrinol Metab1997，82，：	1
6	11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome:clinical scoring system and epigeneticphenotypic correlations显示文摘	Netchine I Rossignol S Dufourg MN		0，，：	1
7	Pituitary stalk interruption syndrome:a clinical-biological-genetic assessment of its pathogenesis显示文摘	Pinto G Netchine I Sobrier ML	1997	J Clin Endocrinol Metab1997，82，：	1
8	IGF-1 molecular anomalies demonstrate its critical role in fetal,postnatal growth and brain development显示文摘	Netchine I Azzi S Le Bouc Y	2011	Best Pract Res Clin Endocrinol Metab2011，25，1：	1
9	Pituitary stalk interruption syndrome: a clinical - biological - genetic assessment of its pathogenesis显示文摘	Pinto G Netchine I Sobrier ML	1997	Clin Endocrinol Metab1997，82，10：	1
10	Ovarian-sparing surgery for ovarian teratoma in children显示文摘	Chabaud-Williamson M Netchine I Fasola S	2011	PediatrBlood Cancer2011，，：	1
11	Pituitary stalk interruption syn- drome:A clinical - biological - genetic assessment of its pathogenesis 显示文摘	Pinto G Netchine I Sobrier ML	1997	J Clin Endocrinol Metab1997，82，10：	1
12	Pathophysiology of syndromic combined pituitary hormone deficiency due to a LHX3 defect in light of LHX3 and LHX4 expression during early human development 显示文摘	Sobrier ML Attie-Bitach T Netchine I	2004	Gene Expr Patterns2004，5，2：	1
13	Pituitary stalk interruption syndrome:a clinical-biological-genetic assessment of its athogenesis显示文摘	Pinto G Netchine I Sobrier ML	1997	J Clin Endocrinol Metab1997，82，10：	1
14	llp15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epige- netic-phenotypic correlations 显示文摘	Netchine I Rossignol S Dufourg MN	2007	J Clin Endocrinol Metab2007，92，8：	1
15	IGF-1 molecular anomalies demonstrate its critical role in fetal,postnatal growth and brain development显示文摘	Netchine I Azzi S Le Bouc Y		0，，1：	1
16	Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency显示文摘	Netchine I Sobrier ML Krude H	2000	Nat Genet2000，25，2：	1
17	Pituitary stalk inter- ruption syndrome: a clinical-biological-genetic assessment of its pathogenesis显示文摘	Pinto G Netchine I Sobrier ML	1997	J Clin Endocrinol Metab1997，82，10：	1
18	Ovarian - sparing surgery for ovarian teratoma in children 显示文摘	Chabaud - Williamson M Netchine I Fasola S	2011	Pediatr Blood Cancer2011，，：	1
19	Syndromic short sta ture in patients with a germline mutation in the LIM ho meoboxLHX4显示文摘	Machinis K Pantel J Netchine I	2001	Am J Hum Genet2001，69，：	1
20	Syndromic short sta- ture in patients with a germline mutation in the LIM ho meoboxLHX4 显示文摘	Maehinis K Pantel J Netchine I	2001	Am J Hum Genet2001，69，：	1

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