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LIANG Y
WANG AH
PROBST FJ
ARHYA IN
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CHEN KS
DESHMUKH D
DOLAN DF
HINNANT JT
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JAIN PK
LALWANI AK
LI XYC
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MOELJOPAWIRO S
MORELL R
NEGRINI C
WILCOX ER
WINATA S
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FRIEDMAN TB
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WILCOX ER
Citation: Pk. Jain et al., A GENE FOR RECESSIVE NONSYNDROMIC SENSORINEURAL DEAFNESS (DFNB18) MAPS TO THE CHROMOSOMAL REGION 11P14-P15.1 CONTAINING THE USHER-SYNDROME TYPE 1C GENE, Genomics, 50(2), 1998, pp. 290-292
Authors:
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CUPPLES LA
ARNOS KS
ASHER JH
BALDWIN CT
BLANTON S
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GREENBERG J
LALWANI AK
MILUNSKY A
NANCE WE
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RAMESAR RS
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WILCOX ER
FARRER LA
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WANG AH
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FRIDELL RA
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CAMPER SA
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LINTHICUM FH
WILCOX ER
MOORE JK
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SANAGUSTIN TB
MISLINSKI J
MILLER MR
SINNINGER Y
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Citation: Pk. Jain et al., A GENE FOR RECESSIVE NONSYNDROMIC SENSORINEURAL HEARING IMPAIRMENT (DFNB18) MAPS TO THE CHROMOSOMAL REGION CONTAINING THE USHER-SYNDROME TYPE 1C GENE, American journal of human genetics, 61(4), 1997, pp. 1632-1632
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RAMESH A
SRISAILAPATHY CRS
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VANCAMP G
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KENYON JB
ZBAR RIS
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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
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RAMESH A
SRISAILAPATHY CRS
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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
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JAIN PK
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DESHMUKH D
RAMESH A
THOMAS E
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Citation: Pk. Jain et al., A HUMAN RECESSIVE NEUROSENSORY NONSYNDROMIC HEARING IMPAIRMENT LOCUS IS A POTENTIAL HOMOLOG OF THE MURINE DEAFNESS (DN) LOCUS, Human molecular genetics, 4(12), 1995, pp. 2391-2394
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LESPERANCE MM
HALL JW
BESS FH
FUKUSHIMA K
JAIN PK
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AGUSTIN TBS
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Citation: Mm. Lesperance et al., A GENE FOR AUTOSOMAL-DOMINANT NONSYNDROMIC HEREDITARY HEARING IMPAIRMENT MAPS TO 4P16.3, Human molecular genetics, 4(10), 1995, pp. 1967-1972
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JAIN PK
DESHMUKH D
THOMAS E
KUMAR S
LALWANI AK
PLOPLIS B
SKARKA H
VERMAN IC
WILCOX ER
Citation: Pk. Jain et al., MAPPING A GENE FOR RECESSIVE NONSYNDROMIC HEARING IMPAIRMENT TO CHROMOSOME 9P21-Q21, American journal of human genetics, 57(4), 1995, pp. 1112-1112
Authors:
LESPERANCE MM
HALL JW
LI X
BESS FH
JAIN PK
PLOPLIS B
SANAUGUSTIN TB
SKARKA H
SMITH RJH
WILLS M
WILCOX ER
Citation: Mm. Lesperance et al., A GENE FOR NONSYNDROMIC HEREDITARY HEARING IMPAIRMENT MAPS TO 4P16.3, American journal of human genetics, 57(4), 1995, pp. 1129-1129
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FEX J
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PLOPLIS B
SANAGUSTIN TB
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Citation: Ak. Lalwani et al., FURTHER ELUCIDATION OF THE GENOMIC STRUCTURE OF PAX3, AND IDENTIFICATION OF 2 DIFFERENT POINT MUTATIONS WITHIN THE PAX3 HOMEOBOX THAT CAUSEWAARDENBURG SYNDROME TYPE-I IN 2 FAMILIES, American journal of human genetics, 56(1), 1995, pp. 75-83
Citation: Er. Wilcox et J. Fex, CONSTRUCTION OF A CDNA LIBRARY FROM MICRODISSECTED GUINEA-PIG CRISTA-AMPULLARIS, Hearing research, 73(1), 1994, pp. 65-66
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LALWANI AK
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FEX J
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SANAGUSTIN T
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Citation: Ak. Lalwani et al., NEW NONSYNDROMIC X-LINKED SENSORINEURAL HEARING IMPAIRMENT LINKED TO XP21.2, American journal of human genetics, 55(4), 1994, pp. 685-694
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ARNOS KS
ASHER JH
BALDWIN CT
DIEHL SR
FRIEDMAN TB
GREENBERG J
GRUNDFAST KM
HOTH C
LALWANI AK
LANDA B
LEVERTON K
MILUNSKY A
MORELL R
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SANAGUSTIN TB
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Citation: La. Farrer et al., LOCUS HETEROGENEITY FOR WAARDENBURG SYNDROME IS PREDICTIVE OF CLINICAL SUBTYPES, American journal of human genetics, 55(4), 1994, pp. 728-737
Authors:
LALWANI AK
BRISTER R
FEX J
GRUNDFAST KM
PLOPLIS B
AGUSTIN TS
SKARKA H
WILCOX ER
Citation: Ak. Lalwani et al., A NEW NONSYNDROMIC X-LINKED SENSORINEURAL HEARING-LOSS LINKED TO XP11.3-21.1, American journal of human genetics, 53(3), 1993, pp. 1027-1027
Authors:
FARRER LA
ASHER JH
BALDWIN CT
FRIEDMAN TB
GREENBERG J
GRUNDFAST KM
LALWANI AK
MILUNSKY A
MORELL R
NEWTON V
RAMESAR R
RAO VS
AGUSTIN TBS
WILCOX ER
WINSHIP I
READ AP
Citation: La. Farrer et al., LOCUS HETEROGENEITY FOR WAARDENBURG SYNDROME IS NOT PREDICTIVE OF CLINICAL SUBTYPES, American journal of human genetics, 53(3), 1993, pp. 1156-1156
Authors:
WILCOX ER
PLOPLIS B
SCHNEIDER M
TACHIBANA M
FEX J
Citation: Er. Wilcox et al., CHARACTERIZATION OF A NOVEL RETINA-SPECIFIC CYCLIC NUCLEOTIDE-GATED CHANNEL, American journal of human genetics, 53(3), 1993, pp. 1633-1633