Liang Y - Search Results

1

Dinucleotide repeat polymorphism at D14S542.

Carey ML, Liang Y, Barber TD, Morell R, Johnson DH, Cox S, Asher JH Jr, Friedman TB. Carey ML, et al. Among authors: liang y. Hum Mol Genet. 1994 Sep;3(9):1712. doi: 10.1093/hmg/3.9.1712-a. Hum Mol Genet. 1994. PMID: 7833943 No abstract available.

2

An informative microsatellite repeat polymorphism in the human neurofilament light polypeptide (NEFL) gene.

Rogaev E, Rogaeva E, Lukiw WJ, Vaula G, Liang Y, Hancock R, McLachlan DC, St George-Hyslop PH. Rogaev E, et al. Among authors: liang y. Hum Mol Genet. 1992 Dec;1(9):781. doi: 10.1093/hmg/1.9.781. Hum Mol Genet. 1992. PMID: 1302625 No abstract available.

3

Congenital non-syndromal autosomal recessive deafness in Bengkala, an isolated Balinese village.

Winata S, Arhya IN, Moeljopawiro S, Hinnant JT, Liang Y, Friedman TB, Asher JH Jr. Winata S, et al. Among authors: liang y. J Med Genet. 1995 May;32(5):336-43. doi: 10.1136/jmg.32.5.336. J Med Genet. 1995. PMID: 7616538 Free PMC article.

4

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

Friedman TB, Liang Y, Weber JL, Hinnant JT, Barber TD, Winata S, Arhya IN, Asher JH Jr. Friedman TB, et al. Among authors: liang y. Nat Genet. 1995 Jan;9(1):86-91. doi: 10.1038/ng0195-86. Nat Genet. 1995. PMID: 7704031

5

Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese population.

Morell R, Liang Y, Asher JH Jr, Weber JL, Hinnant JT, Winata S, Arhya IN, Friedman TB. Morell R, et al. Among authors: liang y. Hum Mol Genet. 1995 Jan;4(1):85-91. doi: 10.1093/hmg/4.1.85. Hum Mol Genet. 1995. PMID: 7711738

6

A highly informative microsatellite repeat polymorphism in intron 1 of the human amyloid precursor protein (APP) gene.

Tupler R, Rogaeva E, Vaula G, Mortilla M, Lukiw W, Liang Y, Hancock R, Rogaev E, St George-Hyslop P. Tupler R, et al. Among authors: liang y. Hum Mol Genet. 1993 May;2(5):620. doi: 10.1093/hmg/2.5.620. Hum Mol Genet. 1993. PMID: 8518820 No abstract available.

7

Human inner ear OCP2 cDNA maps to 5q22-5q35.2 with related sequences on chromosomes 4p16.2-4p14, 5p13-5q22, 7pter-q22, 10 and 12p13-12qter.

Liang Y, Chen H, Asher JH Jr, Chang CC, Friedman TB. Liang Y, et al. Gene. 1997 Jan 15;184(2):163-7. doi: 10.1016/s0378-1119(96)00590-2. Gene. 1997. PMID: 9031623

8

Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.

Innis JW, Asher JH Jr, Liang Y, Wang A, Wilke CM, Dierick HA, Kazen-Gillespie K, Sheldon S, Glover TW, Friedman TB. Innis JW, et al. Among authors: liang y. Am J Med Genet. 1997 Aug 22;71(3):292-7. Am J Med Genet. 1997. PMID: 9268099 Free article.

9

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. Am J Hum Genet. 1998 Apr;62(4):904-15. doi: 10.1086/301786. Am J Hum Genet. 1998. PMID: 9529344 Free PMC article.

10

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

Probst FJ, Fridell RA, Raphael Y, Saunders TL, Wang A, Liang Y, Morell RJ, Touchman JW, Lyons RH, Noben-Trauth K, Friedman TB, Camper SA. Probst FJ, et al. Among authors: liang y. Science. 1998 May 29;280(5368):1444-7. doi: 10.1126/science.280.5368.1444. Science. 1998. PMID: 9603735

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