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Results: 1-8 |
Results: 8
AUTOSOMAL-DOMINANT, PRELINGUAL, NONPROGRESSIVE SENSORINEURAL HEARING-LOSS - LOCALIZATION OF THE GENE (DFNA8) TO CHROMOSOME 11Q BY LINKAGE IN AN AUSTRIAN FAMILY
Authors: KIRSCHHOFER K KENYON JB HOOVER DM FRANZ P WEIPOLTSHAMMER K WACHTLER F KIMBERLING WJ
Citation: K. Kirschhofer et al., AUTOSOMAL-DOMINANT, PRELINGUAL, NONPROGRESSIVE SENSORINEURAL HEARING-LOSS - LOCALIZATION OF THE GENE (DFNA8) TO CHROMOSOME 11Q BY LINKAGE IN AN AUSTRIAN FAMILY, Cytogenetics and cell genetics, 82(1-2), 1998, pp. 126-130
GENOME SEARCH FOR DOMINANT REGRESSIVE HEARING-LOSS
Authors: CHAN CM BEIRAGHI S SMITH SD KENYON JB HOOVER DM KIMBERLING WJ
Citation: Cm. Chan et al., GENOME SEARCH FOR DOMINANT REGRESSIVE HEARING-LOSS, Journal of dental research, 77, 1998, pp. 629-629
GENETIC AND CLINICAL-FEATURES OF SENSORINEURAL HEARING-LOSS ASSOCIATED WITH THE 1555-MITOCHONDRIAL-MUTATION
Authors: USAMI S ABE S KASAI M SHINKAWA H MOELLER B KENYON JB KIMBERLING WJ
Citation: S. Usami et al., GENETIC AND CLINICAL-FEATURES OF SENSORINEURAL HEARING-LOSS ASSOCIATED WITH THE 1555-MITOCHONDRIAL-MUTATION, The Laryngoscope, 107(4), 1997, pp. 483-490
TIETZ-SYNDROME (HYPOPIGMENTATION DEAFNESS) CAUSED BY MUTATION OF MITF/
Authors: SMITH SD KENYON JB KELLEY PM HOOVER D COMER B
Citation: Sd. Smith et al., TIETZ-SYNDROME (HYPOPIGMENTATION DEAFNESS) CAUSED BY MUTATION OF MITF/, American journal of human genetics, 61(4), 1997, pp. 2033-2033
A NOVEL LOCUS FOR AUTOSOMAL-DOMINANT NONSYNDROMIC HEARING-LOSS, DFNA13, MAPS TO CHROMOSOME 6P
Authors: BROWN MR TOMEK MS VANLAER L SMITH S KENYON JB VANCAMP G SMITH RJH
Citation: Mr. Brown et al., A NOVEL LOCUS FOR AUTOSOMAL-DOMINANT NONSYNDROMIC HEARING-LOSS, DFNA13, MAPS TO CHROMOSOME 6P, American journal of human genetics, 61(4), 1997, pp. 924-927
AN AUTOSOMAL RECESSIVE NONSYNDROMIC FORM OF SENSORINEURAL HEARING-LOSS MAPS TO 3P-DFNB6
Authors: FUKUSHIMA K RAMESH A SRISAILAPATHY CRS NI L WAYNE S ONEILL ME VANCAMP G COUCKE P JAIN P WILCOX ER SMITH SD KENYON JB ZBAR RIS SMITH RJH
Citation: K. Fukushima et al., AN AUTOSOMAL RECESSIVE NONSYNDROMIC FORM OF SENSORINEURAL HEARING-LOSS MAPS TO 3P-DFNB6, PCR methods and applications, 5(3), 1995, pp. 305-308
CONSANGUINEOUS NUCLEAR FAMILIES USED TO IDENTIFY A NEW LOCUS FOR RECESSIVE NON-SYNDROMIC HEARING-LOSS ON 14Q
Authors: FUKUSHIMA K RAMESH A SRISAILAPATHY CRS NI L CHEN A ONEILL M VANCAMP G COUCKE P SMITH SD KENYON JB JAIN P WILCOX ER ZBAR RIS SMITH RJH
Citation: K. Fukushima et al., CONSANGUINEOUS NUCLEAR FAMILIES USED TO IDENTIFY A NEW LOCUS FOR RECESSIVE NON-SYNDROMIC HEARING-LOSS ON 14Q, Human molecular genetics, 4(9), 1995, pp. 1643-1648
AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE - LOCALIZATION OF THE 2ND GENE TO CHROMOSOME-4Q13-Q23
Authors: KIMBERLING WJ KUMAR S GABOW PA KENYON JB CONNOLLY CJ SOMLO S
Citation: Wj. Kimberling et al., AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE - LOCALIZATION OF THE 2ND GENE TO CHROMOSOME-4Q13-Q23, Genomics, 18(3), 1993, pp. 467-472
Risultati: 1-8 |