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16篇 您的检索式:作者名="Robin NH"
    题名 作者 年代 出处 被引量
1Mutations in CDMP1 cause autosomal dominant brachydactyly type C显示文摘Polinkovsky A Robin NH Thomas JT 1997Nat Genet1997,17,1:1
2Neuroendocrine changes in patients undergoing whole body hyperthermia显示文摘Robins HI Kalin NH Shelton SE 1987Int J Hyperthermia1987,3,2:1
3Genetic testing for deafness-GJB2 and SLC26A4 as causes of deafness显示文摘Smith RJ Robin NH 2002J Communication Disorders2002,35,4:1
4Stickler syndrome without eye involvement is caused by mutations in COL11A2,the gene encoding the alpha2(XI) chain of type XI collagen显示文摘Sirko-Osadsa DA Murray MA Scott JA Lavery MA Warman ML Robin NH 1998J Pediatr1998,132,:1
5Rise in plasma beta-endorphin,ACTH,and cortisol in cancer patients undergoing whole body hyperthermia显示文摘Robins HI Kalin NH Shelton SE 0,,09:1
6Genetic testing for deafness-GJB2and SLC26A4 as causes of deafness 显示文摘Smitha RJH Robin NH 2002J Commun Disord2002,35,:1
7Mutations in CDMPI causd autosomal dominant brachydaetyly type C显示文摘Polinkovsky A Robin NH Thomas J-F 1997Nat Genet1997,17,:1
8Sibs with Cleidocranial Dyspla sia Born to Normal Parents:Germ Line Mosaicism显示文摘Zackai EH Robin NH McGin DM 1997Am J Med Genet1997,69,4:1
9Amniotic constriction band : a multidisciplinary assessment of etiology and clinical presenta- tion显示文摘Goldfarb CA Sathienkijkanchai A Robin NH 2009J Bone Jont Surg Am2009,91,4:1
10Amniotic constric?tion band: a multidisciplinary assessment of etiology and clinical presentation显示文摘Goldfarb CA Sathienkijkanchai A Robin NH 2009J BoneJoint Surg Am2009,9114,:1
11Clinical and locus heterogeneity in brachydactyly type C显示文摘Robin NH Gunay-Aygun M Polinkovsky A 1997Am J Med Genet1997,68,3:1
12Amniotic constriction band: a muhidisciplinary assessment of etiology and clinical presentation显示文摘Goldfarb CA Sathienkijkanchai A Robin NH 2009J Bone Joint Surg Am2009,914,:1
13Amniotic constric- tion band: a muhidisciplinary assessment of etiology and clinical presentation显示文摘Goldfarb CA Sathienkijkanchai A Robin NH 2009J Bone Joint Surg Am2009,91,4:1
14Neuroendocfine changes in patients undergoing whole body hyperthermia显示文摘Robins HI Kalin NH Shehon SE 1987lnt J Hyperthermia1987,3,2:1
15Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneity显示文摘Robin NH Feldman GJ Mitchell HF 1994Hum Mol Genet1994,3,:1
16Mutations inCDMP1cause autosomal dominant brachydactyly type C显示文摘Polinkovsky A Robin NH Thomas JT 1997Nat Genet1997,17,1:1
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