Authors:
LIANG Y
WANG AH
PROBST FJ
ARHYA IN
BARBER TD
CHEN KS
DESHMUKH D
DOLAN DF
HINNANT JT
CARTER LE
JAIN PK
LALWANI AK
LI XYC
LUPSKI JR
MOELJOPAWIRO S
MORELL R
NEGRINI C
WILCOX ER
WINATA S
CAMPER SA
FRIEDMAN TB
Citation: Y. Liang et al., GENETIC-MAPPING REFINES DFNB3 TO 17P11.2, SUGGESTS MULTIPLE ALLELES OF DFNB3, AND SUPPORTS HOMOLOGY TO THE MOUSE MODEL SHAKER-2, American journal of human genetics, 62(4), 1998, pp. 904-915
Authors:
JAIN PK
LALWANI AK
LI XC
SINGLETON TL
SMITH TN
CHEN A
DESHMUKH D
VERMA IC
SMITH RJH
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:
JAIN PK
LALWANI AK
LI XC
MCDUFFIE T
DESHMUKH D
VERMA IC
WILCOX ER
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
Authors:
LIANG Y
WANG A
MORELL R
WILCOX E
JAIN P
LI XC
NEGRINI C
DESHMUKH D
LUPSKI JR
CHEN KS
HINNANT JT
BARBER T
WINATA S
ARHYA IN
MOELJOPAWIRO S
FRIEDMAN TB
Citation: Y. Liang et al., NONSYNDROMIC RECESSIVE DEAFNESS SEGREGATING WITH DIFFERENT HAPLOTYPESIN FAMILIES FROM BALI AND INDIA MAPPED TO THE 4 CM DFNB3 REGION OF 17P11.2, American journal of human genetics, 61(4), 1997, pp. 1646-1646
Authors:
WISNIEWSKI KE
KIDA E
KACZMARSKI W
DESHMUKH D
MEHTA P
Citation: Ke. Wisniewski et al., IMMUNOCHEMICAL STUDIES OF THE CLN3 PROTEIN, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 96-96
Authors:
JAIN PK
FUKUSHIMA K
DESHMUKH D
RAMESH A
THOMAS E
LALWANI AK
KUMAR S
PLOPLIS B
SKARKA H
SRISAILAPATHY CRS
WAYNE S
ZBAR RIS
VERMAN EC
SMITH RJH
WILCOX ER
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
Authors:
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:
SWAROOP A
FUJITA R
AYON D
DESHMUKH D
BLUMBERG M
SIEVING PA
YANGFENG T
Citation: A. Swaroop et al., IN SEARCH OF X-LINKED RETINITIS-PIGMENTOSA GENE RP3, Investigative ophthalmology & visual science, 35(4), 1994, pp. 1716-1716