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T D Barber

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Gene|October 16, 1999

PAX3 gene structure, alternative splicing and evolutionT D Barber, M C Barber, T E Cloutier, et al.

Journal of Pediatric Urology|March 31, 2009

Prechemotherapy laparoscopic nephrectomy for Wilms' tumorT D Barber, J E Wickiser, D T Wilcox, et al.

Human Molecular Genetics|January 1, 1993

A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1T D Barber, R Morell, D H Johnson, et al.

Journal of Pediatric Urology|June 19, 2016

Results of distal hypospadias repair after pediatric urology fellowship training: A comparison of junior surgeons with their mentorN C Bush, T D Barber, D Dajusta, et al.

The Journal of Biological Chemistry|June 28, 2000

Negative regulation of the serine/threonine kinase B-Raf by AktK L Guan, C Figueroa, T R Brtva, et al.

Biochemistry|July 1, 1999

Chimeric and truncated forms of human complement protein C8 alpha reveal binding sites for C8 beta and C8 gamma within the membrane attack complex/perforin regionM E Plumb, J J Scibek, T D Barber, et al.

Human Molecular Genetics|September 1, 1994

Dinucleotide repeat polymorphism at D14S542M L Carey, Y Liang, T D Barber, et al.

Nature Genetics|January 1, 1995

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17T B Friedman, Y Liang, J L Weber, et al.

Genomics|November 24, 1999

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2Y Liang, A Wang, I A Belyantseva, et al.

American Journal of Human Genetics|June 13, 1998

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.

Pageof 1

Search research articles

Showing results (1-10 of 10) with videos related to

Sort By:

Pageof 1

Gene|October 16, 1999

PAX3 gene structure, alternative splicing and evolutionT D Barber, M C Barber, T E Cloutier, et al.

Journal of Pediatric Urology|March 31, 2009

Prechemotherapy laparoscopic nephrectomy for Wilms' tumorT D Barber, J E Wickiser, D T Wilcox, et al.

Human Molecular Genetics|January 1, 1993

A highly informative dinucleotide repeat polymorphism at the D2S211 locus linked to ALPP, FN1 and TNP1T D Barber, R Morell, D H Johnson, et al.

Journal of Pediatric Urology|June 19, 2016

Results of distal hypospadias repair after pediatric urology fellowship training: A comparison of junior surgeons with their mentorN C Bush, T D Barber, D Dajusta, et al.

The Journal of Biological Chemistry|June 28, 2000

Negative regulation of the serine/threonine kinase B-Raf by AktK L Guan, C Figueroa, T R Brtva, et al.

Biochemistry|July 1, 1999

Chimeric and truncated forms of human complement protein C8 alpha reveal binding sites for C8 beta and C8 gamma within the membrane attack complex/perforin regionM E Plumb, J J Scibek, T D Barber, et al.

Human Molecular Genetics|September 1, 1994

Dinucleotide repeat polymorphism at D14S542M L Carey, Y Liang, T D Barber, et al.

Nature Genetics|January 1, 1995

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17T B Friedman, Y Liang, J L Weber, et al.

Genomics|November 24, 1999

Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2Y Liang, A Wang, I A Belyantseva, et al.

American Journal of Human Genetics|June 13, 1998

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.

Pageof 1