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34篇 您的检索式：作者名="Goodman FR"

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	题名	作者	年代	出处	被引量
1	查看详情显示文摘	Goodman FR		0，，：	1
2	A 117-kb deletion removing HOXD9-HOXD13 and EVX2 cause synpolydactyly显示文摘	Goodman FR Majewski F Collins AL	2002	Am J Hum Genet2002，70，：	1
3	An 147L substitution in the HOXD13 homeodomain causes a rowel humn limb malformation by producing a selective loss of timction显示文摘	Caronia G Goodman FR MoKeown CM el al	2003	Development2003，130，8：	1
4	Rates and risk factors of liver fibrosis progression in patients with chronic hepatitis C显示文摘	Thierry Poynard Vlad Ratziu Frédéric Charlotte Zachary Goodman John McHutchison Janice Albrecht	2001	Journal of Hepatology2001，，：	1
5	Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome显示文摘	Goodman FR Bacchelli C Brady AF	2000	Am J Hum Genet2000，67，：	1
6	Novel HOXA13 mutations and the phenotypic spectrum of hand foot genital syndrome显示文摘	Goodman FR Bacchelli C Brady AF	2000	Am J Hum Genet2000，67，：	1
7	Human HOX genemutations 显示文摘	Goodman FR Scambler PJ	2001	Clin Genet2001，59，1：	1
8	Broad phenotypicspectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families显示文摘	Savarirayan R White SM Goodman FR	2003	Am J Med Genet A2003，117，：	1
9	Limb malformations and the human HOX genes 显示文摘	Goodman FR	2002	AmJ Med Genet2002，112，3：	1
10	HOXA13mu-tations and the Phenotypic spectrum of hand-foot-genitalsyndrome显示文摘	Goodman FR Bacchelli C Brddy AF	2000	Am J Hum Genet2000，67，：	1
11	Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome显示文摘	Goodman FR Bacchelli C Brady AF	2000	Am J Hum Genet2000，67，1：	1
12	Human HOX gene mutations 显示文摘	Goodman FR Scambler PJ	2001	Clin Genet2001，59，1：	1
13	Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis显示文摘	Shears DJ Vassal HJ Goodman FR	1998	Nature Genet1998，19，1：	1
14	Broad pheno- typic spectrum caused by an identical heterozygous CDMP-1 mutation in three unrelated families显示文摘	Savarirayan R White SM Goodman FR	2003	Am J Med Genet A2003，117，2：	1
15	Broad phenotypic spectrum caused by an identical heterozy- gous CDMP-1 mutation in three unrelated families 显示文摘	Savarirayan R White SM Goodman FR	2003	Am J Med Genet A2003，117，2：	1
16	Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract显示文摘	Goodman FR Mundlos S Muragaki Y	1997	Proc Nail Acad Sci U S A1997，94，：	1
17	Limb malformations and the human HOX genes 显示文摘	Goodman FR	2002	Am J Med Genet2002，112，3：	1
18	Broad phe notypic spectrum caused by an identical heterozygous cdmp-1 mutation in three unrelated families显示文摘	Savarirayan R White SM Goodman FR	2003	Am J Med Genet A2003，117，2：	1
19	Synpolydactyly phe notypes correlate with size of expansions in HOXD13 polyalanine tract显示文摘	Goodman FR Mundlos S Muragaki Y	1997	Proe Natl Aead Sci1997，94，14：	1
20	Human HOX gene mutations显示文摘	Scambler PJ	2001	Clin Genet2001，59，：	1

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