Jain PK - Search Results

1

A gene for recessive nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene.

Jain PK, Lalwani AK, Li XC, Singleton TL, Smith TN, Chen A, Deshmukh D, Verma IC, Smith RJ, Wilcox ER. Jain PK, et al. Genomics. 1998 Jun 1;50(2):290-2. doi: 10.1006/geno.1998.5320. Genomics. 1998. PMID: 9653658

2

A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus.

Jain PK, Fukushima K, Deshmukh D, Ramesh A, Thomas E, Lalwani AK, Kumar S, Plopis B, Skarka H, Srisailapathy CR, et al. Jain PK, et al. Hum Mol Genet. 1995 Dec;4(12):2391-4. doi: 10.1093/hmg/4.12.2391. Hum Mol Genet. 1995. PMID: 8634715

3

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

Liang Y, Wang A, Probst FJ, Arhya IN, Barber TD, Chen KS, Deshmukh D, Dolan DF, Hinnant JT, Carter LE, Jain PK, Lalwani AK, Li XC, Lupski JR, Moeljopawiro S, Morell R, Negrini C, Wilcox ER, Winata S, Camper SA, Friedman TB. Liang Y, et al. Among authors: jain pk. Am J Hum Genet. 1998 Apr;62(4):904-15. doi: 10.1086/301786. Am J Hum Genet. 1998. PMID: 9529344 Free PMC article.

4

A gene for autosomal dominant nonsyndromic hereditary hearing impairment maps to 4p16.3.

Lesperance MM, Hall JW 3rd, Bess FH, Fukushima K, Jain PK, Ploplis B, San Agustin TB, Skarka H, Smith RJ, Wills M, et al. Lesperance MM, et al. Among authors: jain pk. Hum Mol Genet. 1995 Oct;4(10):1967-72. doi: 10.1093/hmg/4.10.1967. Hum Mol Genet. 1995. PMID: 8595423

5

Prenatal diagnosis of beta-thalassaemia: experience in a developing country.

Saxena R, Jain PK, Thomas E, Verma IC. Saxena R, et al. Among authors: jain pk. Prenat Diagn. 1998 Jan;18(1):1-7. Prenat Diagn. 1998. PMID: 9483634

6

Genetics in pediatric practice: an Indian perspective.

Verma IC, Mehta L, Jain P. Verma IC, et al. Indian Pediatr. 1991 Sep;28(9):975-82. Indian Pediatr. 1991. PMID: 1802857 No abstract available.

7

Prevention of thalassemia: a necessity in India.

Verma IC, Choudhry VP, Jain PK. Verma IC, et al. Among authors: jain pk. Indian J Pediatr. 1992 Nov-Dec;59(6):649-54. doi: 10.1007/BF02859390. Indian J Pediatr. 1992. PMID: 1340849 No abstract available.

8

Regional distribution of beta-thalassemia mutations in India.

Verma IC, Saxena R, Thomas E, Jain PK. Verma IC, et al. Among authors: jain pk. Hum Genet. 1997 Jul;100(1):109-13. doi: 10.1007/s004390050475. Hum Genet. 1997. PMID: 9225979

9

The tricho-rhino-phalangeal syndromes I and II.

Mehta L, Jain PK, Saxena R, Verma IC. Mehta L, et al. Among authors: jain pk. Indian J Pediatr. 1992 May-Jun;59(3):373-7. doi: 10.1007/BF02821808. Indian J Pediatr. 1992. PMID: 1398874 No abstract available.

10

A new frameshift mutation, insertion of ATCT, at codon 48 in the beta-globin gene causes beta-thalassemia in an Indian proband.

Jain PK, Dozy AM, Verma IC, Chehab FF. Jain PK, et al. Hum Mutat. 1994;3(4):397-8. doi: 10.1002/humu.1380030413. Hum Mutat. 1994. PMID: 8081396 No abstract available.

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