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95篇 您的检索式：作者名="MUNDLOS S"

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	题名	作者	年代	出处	被引量
1	The size of enteric-coated mierospheres influences the intraduodenal lipolytic activity 显示文摘	Kuhnelt P Mundlos S Adler G	1991	Z Gastroenterol1991，29，9：	1
2	The other trinucleotide repeat: polyalanine expansion disorders显示文摘	Albrecht A Mundlos S	2005	Curr Opin Genet Dev2005，15，3：	1
3	Dysehromatosis universalis hereditaria: familial case and ultrastruetural skin investigation显示文摘	Nuber UA Tinschert S Mundlos S	2004	Am J Med Genet A2004，125，3：	1
4	Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia 显示文摘	MUNDLOS S OTTO F MUNDLOS C	1997	Cell1997，89，5：	1
5	The role of sonic hedgehog in vertebrate development 显示文摘	Weed M Mundlos S Olsen B R	1997	Matrix Biol1997，16，2：	1
6	Glucose/galactose malabsorption caused by defect in the Na+/glucose co-transporter显示文摘	Turk E Zabel B Mundlos S	1991	Nature1991，350，6316：	1
7	Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome 显示文摘	Stricker S Verhey van Wijk N Witte F Brieske N Seidel K Mundlos S	2006	Dev Dyn2006，235，12：	1
8	Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia 显示文摘	Mundlos S Otto F Mundlos C	1997	Cell1997，89，5：	1
9	Mutations involving the tran-scription factor CBFA1 cause cleidocranial dysplasia 显示文摘	Mundlos S Otto F Mundlos C	1997	Cell1997，89，5：	1
10	Mutations in the RUNX2 gene in patients with cleidoeranial dysplasia 显示文摘	Otto F Kanegane H Mundlos S	2002	Human Mutation2002，19，3：	1
11	Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia显示文摘	Mundlos S Otto F Mundlos C	1997	Cell1997，89，5：	1
12	Cleidocranial dysplasia: clinical and molecular genetics 显示文摘	Mundlos S	1999	J Med Genet1999，36，3：	1
13	Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation 显示文摘	Nuber UA Tinschert S Mundlos S	2004	Am J Med Goner2004，125，3：	1
14	Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13显示文摘	Muragaki Y Mundlos S Upton J	1996	Science1996，272，：	1
15	Plant nitric oxide synthase:A never-ending story显示文摘	Zemojtel T Frohlich A Palmieri M C Kolanczyk M Mikula I Wyrwicz L S Wanker E E Mundlos S Vingron M Martasek P		0，，：	1
16	Mutations involving thetranscription factor Cbfal cause cleidocranial dysplasia 显示文摘	Mundlos S Otto F Mundlos C	1997	Cell1997，89，：	1
17	Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13 显示文摘	Muragaki Y Mundlos S Upton J	1996	Science1996，272，5261：	1
18	Mutations in the Runx2 gene in patients with eleidocranial dysplasia 显示文摘	Otto F Kanegane H Mundlos S	2002	Human Mutation2002，19，3：	1
19	Mutations in the Runx2 gene in patients with cleidocranial dysplasia显示文摘	Otto F Kanegane H Mundlos S	2002	Hum Mutat2002，19，：	1
20	The receptor tyrosine kinase Ror2 is involved in non-canonical Wnt5a/JNK signalling pathway 显示文摘	Oishi I Suzuki H Onishi N Takada R Kani S Oh- kawara B Koshida I Suzuki K Yamada G Sehwabe GC Mundlos S Shibuya H Takada S Minami Y	2003	Genes Cells2003，8，7：	1

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