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31篇 您的检索式：作者名="BADENAS C"

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	题名	作者	年代	出处	被引量
1	A loss of function model for cystogenesis in human autosomal dominant polycystic kidney disease type2显示文摘	Torra R Badenas C San Millan JL	1999	Am J Hum Genet1999，65，：	1
2	Autosomal recessive Alport's syndrome and benign familial hematuria are collagen type Ⅳdiseases显示文摘	Vega BT Badenas C Ars E	2003	Am J Kidney Dis2003，42，：	1
3	Premature ovarian failure and fragile X female premutation carriers:no evidence for a skewed X-chromosome inactivation pattern显示文摘	Rodriguez-Revenga L Madrigal I Badenas C		MENOPAUSE-THE Journal OF THE NORTH AMERICAN MENOPAUSE SOCIETY0，，：	1
4	Mutational analysis within the 3 region of the PKD1 gene显示文摘	Badenas C Torra R Millan JLS	1999	Kidney Int1999，55，：	1
5	Autosomal dominant polycystic kidney with anticipation and Caroli's disease associated with a PKDI mutation显示文摘	Torra R Badenas C Damell A	1997	Kidney Int1997，52，1：	1
6	Emissivity measurements of several soils and vegetation types in the 8~14 μm wave band:Analysis of two field methods显示文摘	Rubio E V Caselles C Badenas	1997	Remote Sens Environ1997，59，3：	1
7	Clinical,biochemical,and genetic study of 11 patients with erythropoietic protoporphyria including one with homozygous disease显示文摘	Herrero C To-Figueras J Badenas C	2007	Arch Dermatol2007，143，9：	1
8	Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responses 显示文摘	Xuncla M Badenas C Dominguez M	2010	Reprod Biomed Online2010，21，4：	1
9	Pilot study for the neonatal screening of fragile X syndrome 显示文摘	RIFE M MALLOAS J BADENAS C	2002	Prenat Diagn2002，22，6：	1
10	Analysis of CGG variation through 642 meioses in Fragile X families显示文摘	Rife M Badenas C Quinto L	2004	Molecular Human Reproduction2004，10，10：	1
11	Premature ovarian failure and fragile X female premutation carriers: no evidence for a skewed X-chromosome inaetiwttion pattern 显示文摘	Rodriguez-Revenga L Madrigal I Badenas C ct al	2009	Menopause2009，16，5：	1
12	Emissivity measurements of several soils and vegetation types in the 8-14 μm wave band: Analysis of two field methods 显示文摘	Rubio E V Caselles C Badenas	1997	Remote Sens Environ1997，59，3：	1
13	MLPA as first screening method for the detection of microduplications and microdeletions in patients with X-linkod mental retardation显示文摘	Madrigal I Rodriguze RL Badenas C	2007	Genet Med2007，9，2：	1
14	Assessment of QF - PCR as the First Approach in Prenatal Diagnosis显示文摘	Badenas C	2010	J Mol Diagn2010，12，6：	1
15	Screening for FMR1 and FMR2 mutations in 222 individuals from Spanish special schools: identification of a case of FRAXE-associated mental retardation显示文摘	Mila M Sanchez A Badenas C	1997	Hum Genet1997，100，56：	1
16	Assessment of QF-PCR as the first approach in prenatal diagnosis显示文摘	Badenas C Rodrlguez-Revenga L Morales C	2010	J Mol Diagn2010，12，6：	1
17	Linkage,clinical features,and prognosis of autosomal dominant polycystic kidney disease types 1 and 2显示文摘	Torra R Badenas C Darnell A	1996	J Am Soc Nephrol1996，7，：	1
18	Elastin Mutation Screening in a Group of Patients Affected by Vascular Abnormalities 显示文摘	Rodriguez-Revenga L Badenas C Carrio A	2005	Pediatr Cardiol2005，26，：	1
19	Elastln mutation screening in a group of patients affected by vascular abnormalities 显示文摘	Rodriguez-Revenga L Badenas C Carrio A	2005	Pediatr Cardiol2005，26，6：	1
20	Mutations in theCOIAA4 and COL4A3 genes cause familial benign hematuria显示文摘	Badenas C Praga M Taz6n B	2002	J Am Soc Nephrol2002，13，5：	1

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