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A J Mears

Showing results (1-10 of 17) with videos related to

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American Journal of Human Genetics|October 27, 1997
Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25D B Gould, A J Mears, W G Pearce, et al.
Ophthalmology|November 1, 1996
Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinctM A Walter, F Mirzayans, A J Mears, et al.
Journal of Medical Genetics|November 1, 1996
Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22A J Dawson, A J Mears, A E Chudley, et al.
American Journal of Human Genetics|July 1, 1997
Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanningF Mirzayans, A J Mears, S W Guo, et al.
American Journal of Human Genetics|December 1, 1996
Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25A J Mears, F Mirzayans, D B Gould, et al.
American Journal of Human Genetics|September 1, 1995
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical regionA J Mears, H el-Shanti, J C Murray, et al.
Human Molecular Genetics|February 1, 1994
The E subunit of vacuolar H(+)-ATPase localizes close to the centromere on human chromosome 22V Baud, A J Mears, V Lamour, et al.
NPJ Genomic Medicine|December 22, 2017
Mining the transcriptome for rare disease therapies: a comparison of the efficiencies of two data mining approaches and a targeted cell-based drug screenA J Mears, S C Schock, J Hadwen, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25F Mirzayans, D B Gould, E Héon, et al.
Novartis Foundation Symposium|January 31, 2004
From disease genes to cellular pathways: a progress reportJ Yu, A J Mears, S Yoshida, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
American Journal of Human Genetics|October 27, 1997
Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25D B Gould, A J Mears, W G Pearce, et al.
Ophthalmology|November 1, 1996
Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinctM A Walter, F Mirzayans, A J Mears, et al.
Journal of Medical Genetics|November 1, 1996
Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22A J Dawson, A J Mears, A E Chudley, et al.
American Journal of Human Genetics|July 1, 1997
Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanningF Mirzayans, A J Mears, S W Guo, et al.
American Journal of Human Genetics|December 1, 1996
Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25A J Mears, F Mirzayans, D B Gould, et al.
American Journal of Human Genetics|September 1, 1995
Minute supernumerary ring chromosome 22 associated with cat eye syndrome: further delineation of the critical regionA J Mears, H el-Shanti, J C Murray, et al.
Human Molecular Genetics|February 1, 1994
The E subunit of vacuolar H(+)-ATPase localizes close to the centromere on human chromosome 22V Baud, A J Mears, V Lamour, et al.
NPJ Genomic Medicine|December 22, 2017
Mining the transcriptome for rare disease therapies: a comparison of the efficiencies of two data mining approaches and a targeted cell-based drug screenA J Mears, S C Schock, J Hadwen, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25F Mirzayans, D B Gould, E Héon, et al.
Novartis Foundation Symposium|January 31, 2004
From disease genes to cellular pathways: a progress reportJ Yu, A J Mears, S Yoshida, et al.
Pageof 2