维普期刊资源整合服务平台（V6.5）

1479篇 您的检索式：期刊名="Genetic a"

选中清除导出查看参考文献查看引证文献引用追踪共74页首页上一页第1页下一页末页 /74 跳转

	题名	作者	年代	出处	被引量
1	A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostoses显示文摘	Fryns JP Devriendt K	2004	Am J Med Genet A2004，128，：	1
2	Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency显示文摘	Seidahmed MZ Alyamani EA Rashed MS	2005	Am J Med Genet A2005，136，2：	1
3	Omphalocele and gastros- chisis and associated malformations 显示文摘	Stoll C Alembik Y Dott B	2008	Am J Med Genet A2008，146，10：	1
4	Variation in IRF6con-tributes to nonsyndromic cleft lip and palate显示文摘	Blanton SH Cortez A Stal S	2005	Am J Med Genet A2005，137，3：	1
5	Maternal inheritance in cyclic vomiting syndrome显示文摘	Boles RG Adams K Li BU	2005	Am J Med Genet A2005，133，1：	1
6	Genetic susceptibilities inthe association between maternal exposure to tobacco smoke andthe risk of nonsyndromic oral cleft显示文摘	Chevrier C Bahuau M Perret C	2008	Am J Med Genet A2008，146，18：	1
7	Clinical and epidemiological findings in patients with central ray deficiency split hand foot malformation (SHFM) in Manitoba, Canada显示文摘	Elliott AM Reed MH Chudley AE	2006	Am J Med Genet A2006，140，：	1
8	Is Dandy-Walker mal formation associated with 'distal 13q deletion syn drome'? Findings in a fetus supporting previous observation显示文摘	Alanay Y Aktas D Utine E	2005	Am J Med Genet A2005，136，3：	1
9	Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysms显示文摘	Regalado E Medrek S Tran-Fadulu V	2011	Am J Med Genet A2011，155，9：	1
10	Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes 显示文摘	Shaw GM Iovannisci DM Yang W	2005	Am J Med Genet A2005，138，1：	1
11	Large deletions and uniparental disomy detected by SNP arrays in adults with thoracic aortic aneurysms and dissections 显示文摘	Prakash S Lemaire SA Bray M	2010	Am J Med Genet A2010，152，9：	1
12	PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations显示文摘	Avila JR Jezewski PA Vieira AR	2006	Am J Med Genet A2006，140，23：	1
13	Sudden infant death syndrome:Review of implicated genetic factors显示文摘	Weese-Maye D E Aekerman M J Marazita M L	2007	American Journal of Medical Genetics Part A2007，143，：	1
14	Diploid sperm produced by artificially sex-reversed clone loaches 显示文摘	Yoshikawa H Morishima K Kusuda S	2007	J Exp Zool Part A Ecol Genet Physiol2007，307，2：	1
15	Clinical and molecular characterization of individuals with 18p deletion: a geno- type-phenotype correlation 显示文摘	Wesler U Bondeson ML Edeby C	2006	Am J Med Genet A2006，140，：	1
16	Risk factors for isolated biliary atresia, National Birth Defects Prevention Study, 1997-2002显示文摘	THE N S HONEIN M A CATON A R	2007	Am J Med Genet A2007，143，19：	1
17	Using the shifted multiplicative model to search for 'separability'in crop cultivar trials显示文摘	Cornelius P L Seyedsatr M S Crossa J	1992	Theor A ppl Genet1992，84，：	1
18	Minor malformations characteristic of the retinoic acid embryopathy and other birth outcomes in children of women exposed to topical tretinoin dur- ing early pregnancy显示文摘	Loureiro KD Kao KK Jones KL	2005	Am J Med Genet A2005，136，2：	1
19	Deletion of JAM C,a candidate gene {or heart defects in Jacobsen syndrome, results in a normal cardiac pbenotype in mice显示文摘	Ye M Hamzeh R Geddis A	2009	Am I Med Genet A2009，149，7：	1
20	miRNA mutations arenot a common cause of deafness 显示文摘	Hildebrand M S Witmer P D Xu S	2010	Am J Med Genet A2010，152，3：	1

返回顶部每页显示：

共74页首页上一页第1页下一页末页 /74 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示