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39篇 您的检索式：作者名="Grundfast"

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	题名	作者	年代	出处	被引量
1	Delayed diagnosis and fate of congenital chholesteatoma显示文摘	Ahuja GS Parisier SC	1995	Arch Otolaryngol Head Neck Surg1995，121，：	1
2	Ma jor and minor temporal bone abnormalities in children with and without congenital sensorineural hearing loss 显示文摘	JOHN E TANDY R GRUNDFAST K	2002	Arch Otolaryngol Head Neck Surg2002，128，：	1
3	Major and minor temporal bone abnormalities in children with and without congenital sensorineutal hearing loss 显示文摘	McClay JE Tandy R Grundfast K	2002	Arch Otolaryngol Head Neck Surg2002，128，6：	1
4	Major and minor temporal bone abnormalities in children with and without congenital sensorineural hearing loss显示文摘	McClay JE Tandy R Grundfast K	2002	Arch Otolaryngol Head Neck Surg2002，128，6：	1
5	Diagnosis and management of spontaneous cerebrospinal fluid-middle ear effusion and otorrhea显示文摘	BROWN N E GRUNDFAST K M JABRE A	2004	Laryngoscope2004，114，：	1
6	Clinical practice guideline: otitis media with effusion显示文摘	Richard M Rosenfeld Larry Culpepper Karen J Doyle Kenneth M Grundfast Alejandro Hoberman Margaret A Kenna Allan S Lieberthal Martin Mahoney Richard A Wahl Charles R Woods Barbara Yawn	2004	Otolaryngology - Head and Neck Surgery2004，，5：	1
7	Major and minor temporal bone abnormalities in children with and without congenital senso- rineural hearing loss显示文摘	McClay JE Tandy R Grundfast K	2002	Arch Otolaryngol Head Neck Surg2002，128，6：	1
8	Major and minor temporal bone abnormalities in children with and without congenital sensorineuralhearing loss 显示文摘	Mc Clay JE Tandy R Grundfast K	2002	Arch Otolaryngol Head Neck Surg2002，128，6：	1
9	Waardcnburg syndrome(WS) type I is caused by defects at multiple loci,one of which is near AL PP on chromosome:fist report of the WS consorlium 显示文摘	Farrcr LA Grundfast KM Amos L	1992	Am J Hum Genet1992，50，：	1
10	Major and minor tempo- ral bone abnormalities in children with and without congenital sensorineural hearing loss 显示文摘	McClay JE Tandy R Grundfast K	2002	Arch Otolaryngol Head Neck Surg2002，128，6：	1
11	Mutation of atranscription factor,TFCP2L3,causes progressive au-tosomal dominant hearing loss,DFNA28显示文摘	Peters L M Anderson D W Griffith A J Grundfast KM San Agustin T B Madeo A C	2002	Hum MolGenet2002，11，：	1
12	A stepwise opproach ofthe diagnosis and treatment of heredity hearing loss 显示文摘	TOMASKI SM GRUNDFAST KM	1999	Pedatr Clin North1999，46，：	1
13	Emerging therapies for the treatment and prevention of otitis media显示文摘	Aliphas A Prufer N Grundfast KM	2006	Expert OpinEmergDrugs2006，11，2：	1
14	Major and minor temporal bone abnormalities in children with and without congenital sensorineural hearing loss 显示文摘	McClay JE Tandy R Grundfast K	2002	Arch Otolaryngol Head Neck Surg2002，128，6：	1
15	Diagnosis and management of spontaneous cerebrospinal fluid-middle ear effusion and otorrhea显示文摘	Brown N E Grundfast K M Jabre A	2004	Laryngoscope2004，114，5：	1
16	A stepwise approach of the diag- nosis and treatment of heredity hearing loss 显示文摘	Tomaski SM Grundfast KM	1999	Pediatr Clin North Am1999，46，1：	1
17	Waardenburg Syndrome (WS) Type Ⅰ is Caused by Defects at Multiple Foci, One of Which is Near ALPP On Chromosome 2 : First Report of the WS Consortium显示文摘	Farrer LA Grundfast KM Amos J et ai	1992	Am J Hum Genet1992，50，5：	1
18	Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near AL PP on chromosome: first report of the WS consortium 显示文摘	Farrer LA Grundfast KM Amos J	1992	Am J Hum Genet1992，50，：	1
19	Waardenburg syndrome(WS)typeⅠis caused by defects at multiple loci,one of which is near ALPP on chromosome 2:first report of the WS consortium显示文摘	Farrer LA Grundfast KM Amos J	1992	Am J Hum Genet1992，50，：	1
20	Waardenburg syndrome(WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome2 : first report of the WS consortium 显示文摘	FARRER L A GRUNDFAST K M AMOS J	1992	Am J Hum Genet1992，50，：	1

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