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10篇 您的检索式：作者名="Moya CM"

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		题名	作者	年代	出处	被引量
	1	Two distinct compound heterozygous constellation (R277X/IVS34-1G 1C and R277X/R1511X) in the thyroglobulin (TG) gene in affected individuals of a Brazilian kindred with congenital goiter and defective TG synthesis显示文摘	Gutnisky VJ Moya CM Rivolta CM		0，，：	1
	2	The thyroid as a model for molecular mechanisms in genetic diseases显示文摘	Rivolta CM Moya CM Esperante SA		0，，：	1
	3	Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G1 A[R2223H]) resulting in fetal goitrous hypothyroidism显示文摘	Caron P Moya CM Malet D		0，，：	1
	4	Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725GA ) resulting in fetal goitrous hypothyroidism显示文摘	Caron P Moya CM Malet D	2003	J Clin Endocrinol Metab2003，88，：	1
	5	Genotyping and characterization of two polymorphic microsatellite markers located within introns 29 and 30 of the human thyroglobulin gene显示文摘	Rivolta CM Moya CM Mendive FM	2002	Thyroid2002，12，：	1
	6	Two distinct com-pound heterozygous constellation (R277X/ IVS34-1G 1 C andR277X/R151IX) in the thyroglobulin (TG) gene in affected in-dividuals of a Brazilian kindred with congenital goiter and defec-tive TG synthesis 显示文摘	Gutnisky VJ Moya CM Rivolta CM	2004	J Clin Endocrinol Metab2004，89，2：	1
	7	The thyroid as a model for molecular mechanisms in genetic diseases 显示文摘	Rivolta CM Moya CM Esperante SA	2005	Medicina ( B Aires )2005，65，3：	1
	8	WNT/beta-catenin increases the production of incretins by entero-endocrine cells显示文摘	García-Martínez JM Chocarro-Calvo A Moya CM	2009	Diabetologia2009，52，9：	1
	9	Genomic organization of the human thyroglobulin gene:the complete intron-exon structure显示文摘	Fernando FM Rivolta CM Moya CM	2001	Eur J Endocrinol2001，145，4：	1
	10	Compound heterozygous mutations in the thyroglobulin gene (1143delC and 6725G-A) resulting in fetal goitrous hypothyroidism显示文摘	Caron P Moya CM Malet D	2003	J Clin Endocrinol Metab2003，88，8：	1

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