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35篇 您的检索式：作者名="Burlet P"

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	题名	作者	年代	出处	被引量
1	Anovel association of the SMN protein with two major non-ribosomal mucleolar proteins and its implication in spinal muscular atrophy显示文摘	Lefebvre S Burlet P Viouet L	2002	Hum Mol Genet2002，11，9：	1
2	Identification and characterization of a spinal muscular atrophy-determining gene显示文摘	Leeibvres S Burglen L Reboullet S Clermont O Burlet P Viollet L	1995	Cell1995，80，1：	1
3	Netrtron dif- fraction study of magnetic structures in TbNiAl 显示文摘	Javorsky P Burlet P Sechovsky V	1997	J Magn Magn Mater1997，166，1：	1
4	Effects of long - term ingestion of aspartame on hypotbalamic neuropeptide Y, plasma leptin and body weight gain and composition 显示文摘	Beck B Burlet A Max J P	2002	Physiol Behav2002，75，12：	1
5	Anovel association of the SMN protein with two major non - ribosomal mucleolar proteins and its implication in spinal muscular atropliy显示文摘	Iefebvre S Burlet P Viouet L	2002	Hum Mol Genet2002，11，9：	1
6	Refined linkage map of chromosome 5 in the region of the spinal muscular atrophy gene显示文摘	Melki J Burlet P Clermont O	1993	Genomics1993，15，3：	1
7	Preimplantation genetic diagnosis for autosomal recessive polycystic kidney disease 显示文摘	Gigarel N Frydman N Burlet P	2008	Reprod Biomed Online2008，16，1：	1
8	Correlation between severity and SMN protein level in spinal muscular atrophy显示文摘	Lefebvre S Burlet P Liu Q Bertrandy S Clermont O Munnich A	1997	Nat Genet1997，16，3：	1
9	Multiple displacement am- plification improves PGD for fragile X syndrome 显示文摘	Burlet P Frydman N Gigarel N	2006	Mol Hum Re- prod2006，12，10：	1
10	Prenatal prediction of Werdning-Hoffmann disease using linked polymorphic DNA probes显示文摘	Melki J Abdelhak S Burlet P	1992	Med Genet1992，29，3：	1
11	Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes显示文摘	Melki J Abdelhak S Burlet P	1992	J Med Genet1992，29，3：	1
12	Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highlypolymorphic DNA markers显示文摘	Clermont O Burlet P Burglen L	1994	Am J Hum Genet1994，54，4：	1
13	Multiple displacement amplification improves PGD for fragile X syndrome 显示文摘	Burlet P Frydman N Gigarel N	2006	Mol Hum Reprod2006，12，10：	1
14	Identification and characterization of a spinal muscular atrophy-determining gene显示文摘	Lefebvre S Burglen L Reboullet S Clermont O Burlet P Viollet L	1995	Cell1995，80，1：	1
15	Preimplantation genetic diagnosis for autosomal recessive polycystic kidney disease显示文摘	Gigarel N Frydman N Burlet P	2008	Reprod Biomed Online2008，16，1：	1
16	Large Scale deletion of the 5q13 region are specific to Werdnig-Hoffman disease显示文摘	Burlet P Burglen L Clermont O	1996	Med Genet1996，33，：	1
17	The RNA-binding properties of SMN: deletion analysis of the zebrafish orthologue defines domains conserved in evolution 显示文摘	Burlet P Clermont O	1999	Hum Mol Genet1999，8，：	1
18	Prenatal prediction of Werdning-hoffmann disease using linked polymorphic DNA probes显示文摘	Melki J Abdelha K S Burlet P	1992	J Med Genet1992，29，3：	1
19	查看详情显示文摘	Burlet P Flouquet J Genicon J L		0，，：	1
20	Multiple displacement amplification improves PGD for fragile X syndrome显示文摘	Burlet P Frydman N Gigarel N	2006	Mol Hum Reprod2006，12，：	1

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