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Results: 1-8 |
Results: 8
GENETIC-MAPPING REFINES DFNB3 TO 17P11.2, SUGGESTS MULTIPLE ALLELES OF DFNB3, AND SUPPORTS HOMOLOGY TO THE MOUSE MODEL SHAKER-2
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
A GENE FOR RECESSIVE NONSYNDROMIC SENSORINEURAL DEAFNESS (DFNB18) MAPS TO THE CHROMOSOMAL REGION 11P14-P15.1 CONTAINING THE USHER-SYNDROME TYPE 1C GENE
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
A GENE FOR RECESSIVE NONSYNDROMIC SENSORINEURAL HEARING IMPAIRMENT (DFNB18) MAPS TO THE CHROMOSOMAL REGION CONTAINING THE USHER-SYNDROME TYPE 1C GENE
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
NONSYNDROMIC RECESSIVE DEAFNESS SEGREGATING WITH DIFFERENT HAPLOTYPESIN FAMILIES FROM BALI AND INDIA MAPPED TO THE 4 CM DFNB3 REGION OF 17P11.2
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
IMMUNOCHEMICAL STUDIES OF THE CLN3 PROTEIN
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
A HUMAN RECESSIVE NEUROSENSORY NONSYNDROMIC HEARING IMPAIRMENT LOCUS IS A POTENTIAL HOMOLOG OF THE MURINE DEAFNESS (DN) LOCUS
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
MAPPING A GENE FOR RECESSIVE NONSYNDROMIC HEARING IMPAIRMENT TO CHROMOSOME 9P21-Q21
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
IN SEARCH OF X-LINKED RETINITIS-PIGMENTOSA GENE RP3
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
Risultati: 1-8 |