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47篇 您的检索式：作者名="EIBERG H"

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	题名	作者	年代	出处	被引量
1	Analysis of connexin expression during mouse Schwann cell development identifies connexin29 as a novel marker for the transition of neural crest to precursor cells显示文摘	Li J Habbes H W Eiberger J	2007	Glia2007，55，1：	1
2	Variation in CAPN10 in relation to type 2 diabetes,obesity and quantitative metabolic traits:studies in 6018 whites显示文摘	Jensen D Urhammer S A Eiberg H	2006	Mol Genet Meta2006，89，4：	1
3	Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6显示文摘	Eiberg H Bixler D Nielsen L S	1987	Clin Genet1987，32，2：	1
4	Cytoplasmic expression of E-cadherin and beta-catenin correlated with LOH and hypermethylation of the APC gene in oral squamous cell carcinomas显示文摘	Gao S Eiberg H Krogdahl A	2005	J Oral Pathol Med2005，34，2：	1
5	Assignment of dominant inherited noctumal enuresis(ENUR1)to chromosome 13q显示文摘	Eiberg H Berendt I Mohr J	1995	Nat Genet1995，10，：	1
6	Cytoplasmic expression of Ecadherin and β-Catenin correlated with LOH and hypermethylation of the APC gene in oral squamous cell carcinomas 显示文摘	Gao S Eiberg H Krogdahl A	2005	J Oral Pathol Med2005，34，2：	1
7	Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression 显示文摘	Eiberg H Troelsen J Nielsen M	2008	Hum Genet2008，123，2：	1
8	Identity of the polymorphisms for esterase D and Sformylglutathione hydrolase in red blood cells显示文摘	EIBERG H MOHR J	1986	Hum Genet1986，74，：	1
9	Comparison of the polymerase chain reaction using genus specific oligonucleotide primers and microbiology culture for the detection of Salmonella in dragswabs from poultry houses显示文摘	Cohen N D W allis D E N eibergs H L	1994	Poult Sci1994，73，8：	1
10	Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2gene inhibiting OCA2 expression显示文摘	Eiberg H Troelse J N Nielsen M	2008	Hum Genet2008，123，：	1
11	Cytoplasmic expression of E-cadherinand beta-catenin correlated with LOH and hypermethylation of the APCgene in oral squamous cell carcinomas显示文摘	Gao S Eiberg H Krogdahl A	2005	Oral Pathol Med2005，34，2：	1
12	Blue eye color in humans may be caused by a perfectly asso- ciated founder mutation in a regulatory element lo- cated within the HERC2 gene inhibiting OCA2 ex- pression显示文摘	Eiberg H Troelsen J Nielsen M	2008	Hum Genet2008，123，2：	1
13	Maximum oxygen uptake and objectively measured physical activity in Danish children 6-7 years of age: the Copenhagen school child intervention study显示文摘	Eiberg S Hasselstrom H Gronfeldt V	2005	Br J Sports Med2005，39，10：	1
14	Genetic heterogeneity in microcornea-cataract:five novel mutations in CRYAA,CRYGD,and GJA8 显示文摘	Hansen L Yao W Eiberg H	2007	Invest Ophthahnol Vis Sci2007，48，：	1
15	Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract显示文摘	Bu L Jin YP Shi YF Chu R Ban A Eiberg H	2002	Nature Genetics2002，31，7：	1
16	Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract显示文摘	Bu L Jin Y Shi Y Chu R Ban A Eiberg H	2002	Nature Genetics2002，31，7：	1
17	Clinical cancer advances 2005:major research advances in cancer treat-ment,prevention ant]screaning-a report from the Aameriean Society of Clinical Oneology显示文摘	BAJORIN D F BI EIBERG H et a1	2006	J Clin Oncol2006，24，1：	1
18	Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression显示文摘	EIBERG H TROELSEN J NIELSEN M	2008	Hum Genet2008，123，2：	1
19	A novel nonsense mutation in MYO6 is associated with progres-sive nonsyndromic hearing loss in a Danish DFNA22 family显示文摘	Sanggaard KM Kjaer KW Eiberg H Nürnberg G Nürnberg P Hoffman K Jensen H S?rum C Rendtorff ND Tranebjaerg L		0，，08：	1
20	Assignment of dominant inherited nocturnal enuresis (ENUR1) to chromosome 13q显示文摘	Eiberg H Berendt I Mohr J	1995	Nat Genet1995，10，：	1

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