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21篇 您的检索式：作者名="Robinson DO"

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	题名	作者	年代	出处	被引量
1	Further evidence for an imprinted gene for neonatal diabetes localized to chromosome 6q22-q23 显示文摘	Temple IK Gardner R J Robinson DO	1996	Hum Mol Genet1996，5，8：	1
2	Oculopharyngeal muscular dystrophy (OPMD):analysis of the PABPN1 gene ex- pansion sequence in 86 patients reveals 13 different expansion types and further evidence for unequal recombination as the mutational mechanism显示文摘	Robinson DO Hammans SR Read SP	2005	Hum Genet2005，116，4：	1
3	Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23显示文摘	Temple IK Gardner RJ Robinson DO		0，，08：	1
4	Genetic analysis of chro- mosome I 1 p13 and the PAX6 gene in a series of 125 eases re- ferred with aniridia显示文摘	ROBINSON DO HOWARTH R J WILLIAMSON KA VAN HEY- NINGEN V BEAL S J CROLLA JA	2008	Am J Med Genet A2008，146，5：	1
5	The origin of the extra Y chromosome in males with a 47, XYY karyotype 显示文摘	Robinson DO Jacobs PA	1999	Hum Mol Genet1999，8，12：	1
6	Genetic a- nalysis 'of chromosome 11 pl 3 and the PAX6 gene in a series of 125 cases referred With aniridia显示文摘	Robinson DO Howarth R J Williamson KA	2008	Am J Med Genet A2008，146，5：	1
7	Genetic analysis of chromosome 1 lpl3 and the PAX5 gene in series of 125 cases referred with aniridia显示文摘	Robinson DO Howarth R J Williamson KA van Heyningen V Beal SJ Crolla JA	2008	Am J Med Genet A2008，146，5：	1
8	In vivo E-selectin upregulation correlates early with infiltration of PMN,later with PBL entry:MAbs block both显示文摘	Binns RM Licence ST Harrison AA Keelan ET Robinson MK Haskard DO	1996	Am J Physiol1996，270，：	1
9	Fceding critically ill patients:Current concepts显示文摘	Trujillo EB Robinson MK Jacobs DO	2001	Crit Care Nurse2001，21，4：	1
10	The origin of the extra Y chromosome in males with a 47,XYY karyotype显示文摘	Robinson DO Jacobs PA	1999	Hum Mol Genet1999，8，：	1
11	The origin of the extra Y chromosome in males with a 47, XYY karyotype 显示文摘	Robinson DO Jacobs PA	1999	Hum Mol Genet1999，8，：	1
12	Oculopharyngeal muscular dystrophy (OPMD): analysis of the PABPN1 gene ex- pansion sequence in 86 patients reveals 13 different expansiontypes and further evidence for unequal recombination as the mu- tational mechanism显示文摘	Robinson DO Hammans SR Read SP	2005	Hum Genet2005，116，4：	1
13	Transient neonatal diabetes mellitus in an infant with paternal uniparental disomy of chromosome 6 including heterodisomy for 6q24显示文摘	Milenkovic T Martic J Robinson DO	2006	J Pediatr Endocrinol Metab2006，19，11：	1
14	A case of rare recessive ocalopharyngeal muscular dystrophy (OPMD) coexisting with hereditary neuropathy with liability to pressure palsies (HNPP)显示文摘	Marsh EA Robinson DO	2008	Clin Neurol Neurosurg2008，110，：	1
15	Feeding critically ill patients: current concepts显示文摘	Trujillo EB Robinson MK Jacobs DO	2010	Critical Care Nurse2010，21，4：	1
16	In vivo E-selectin upregulation correlates early with infiltration of PMN,later with PBL entry: MAbs block both 显示文摘	Binns RM Licence ST Harrison AA Keelan ET Robinson MK Haskard DO	1995	Am J Physiol1995，270，12：	1
17	Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophy显示文摘	Bunyan DJ Robinson DO Collins AL	1994	Hum Genet1994，93，5：	1
18	Tissue engineering:current challenges and expanding opportunities显示文摘	Butnariu-Ephrat M Robinson D Mendes DO	2001	Clin Orthop2001，630，2：	1
19	Feeding critically ill patients: current concepts显示文摘	Robinson MK Jacobs DO	2001	Crit Care Nurse2001，21，4：	1
20	Genetic analysis of chromosome 1 lp13 and the PAX6 gene in a series of 125 cases referred with aniridia显示文摘	Robinson DO Howarth RJ Williamson KA	2008	Am J Med Genet A2008，146，：	1

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