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18篇 您的检索式：期刊名="Hum Molee Genet"

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		题名	作者	年代	出处	被引量
	1	Defects in human methionine synthase in cblG patients显示文摘	Gulati S Baker PJ Li YN	1996	Hum Mole Genet1996，12，：	1
	2	Cloning,mapping and RNA analysis of the human methionine synthase gene显示文摘	Li YN Gulati S Baker PJ	1996	Hum Mole Genet1996，12，：	1
	3	Human methionine synthase:cDNA cloning and identification of mutations in patients of cbl G complementation group of folate/cobalam in disorders显示文摘	Leclerc D Campeau E Goyette P	1996	Hum Mole Genet1996，5，12：	1
	4	The UTX gene escapes X inactivation in mice and humans显示文摘	Carrel L Pennisi D Philippe C Quaderi N Siggers P Steiner K Tam P P Monaco A P Willard H F Koopman P	1998	Hum Moles Genet1998，7，：	1
	5	Human methionine synthase:cDNA clonong and identification of mutations in patients of cb/G com plementation group of folate/cobalam in disorders显示文摘	Leclerc D Campeau E Goyette P	1996	Hum Mole Genet1996，12，：	1
	6	Tissue and linenge-specific variation in inactive X chromosome expression of the murine Smcx gene显示文摘	Hunt P A Willard H F	1996	Hum Molee Genet1996，5，9：	1
	7	The mouse Smcx gene exhibits developmental and tissue specific variation in degree of escape from X inactivation显示文摘	Norris D Fisher A Brockdorff N	1996	Hum Mole Genet1996，5，：	1
	8	Human methionine synthase:cDNA cloning and identification of mutations in patients of cb/G comple mentation group of folate/cobala min disorders显示文摘	Leclerc D Campeau E Goyette P	1996	Hum Mole Genet1996，12，：	1
	9	Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9 显示文摘	Robertson NG Resendes BL Lin JS	2001	Hum Molee Genet2001，10，：	1
	10	Human methionine synthase:cDNA cloning and identification of mutations in patients of cb1G complementation group of folate/cobalamin disorders显示文摘	Leclerc D Campeau E Goyette P	1996	Hum Mole Genet1996，12，12：	1
	11	Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious puberty显示文摘	Van Dop C Geffner M E	1995	Hum Mole Genet1995，，4：	1
	12	Telmerase and cancer显示文摘	Shay JW Zou Y Hiyama E	2001	Hum Mole Genet2001，10，7：	1
	13	Human methionine synthase:cDNA cloning and identification of mutations in patients of cb/Gcomplementation group of folate/cobalamin disorders 显示文摘	Leclerc D Campeau E Goyette P	1996	Hum Mole Genet1996，12，：	1
	14	Human methionine synthase:cDNA cloning and identification of mutations in patients of cb1G complementation group of folate/cobalam in disorders显示文摘	Leclerc D Campeau E Goyette P	1996	Hum Mole Genet1996，5，12：	1
	15	FOXL2 disruption causes mouse ovarian failure by pervasive blockage of follicle development显示文摘	Manuela Uda Chris Ottolenghi Laura Crisponi	2004	Hum Mole Genet2004，13，11：	1
	16	A genomic rearrangement resulting in a tandem duplication is associated with splithand-split foot malformation 3 (SI-IFM3) at10q24显示文摘	De Mollerat XJ Gurrieri F Morgan CT	2003	Hum Molee Genet2003，12，：	1
	17	Telomerase and cancer显示文摘	Shay JW Zou Y Hiyama E	2001	Hum Mole Genet2001，10，7：	1
	18	Human methionine synthase:cDNA cloning and identification of mutations in patients of cb/G complementation group of folate/cobalamin disorders显示文摘	Leclerc D Campeau E Goyette P	1996	Hum Mole Genet1996，12，：	1

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