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T A Maher

Showing results (1-10 of 12) with videos related to

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Genetic Testing|July 14, 2007
The value of MLPA in Waardenburg syndromeJ M Milunsky, T A Maher, M Ito, et al.
American Journal of Medical Genetics|May 9, 2001
Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paragangliomaJ M Milunsky, T A Maher, V V Michels, et al.
Genetic Testing|February 24, 2001
Connexin-26 gene analysis in hearing-impaired newbornsJ M Milunsky, T A Maher, E Yosunkaya, et al.
Clinical Genetics|April 25, 2006
LADD syndrome is caused by FGF10 mutationsJ M Milunsky, G Zhao, T A Maher, et al.
American Journal of Obstetrics and Gynecology|March 1, 1991
Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probesA Milunsky, J C Skare, J M Milunsky, et al.
Clinical Genetics|June 7, 2003
XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's diseaseJ M Milunsky, T A Maher, B A Loose, et al.
Clinical Genetics|March 14, 2008
A re-examination of the chromosome 8p22-8p23.1 region in Kabuki syndromeJ M Milunsky, T A Maher, G Zhao, et al.
Prenatal Diagnosis|November 23, 2005
The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysisA Milunsky, C Konialis, S H Shim, et al.
Genetic Testing|April 19, 2002
Mutation analysis in Rett syndromeJ M Milunsky, R V Lebo, T Ikuta, et al.
Clinical Genetics|September 27, 2007
Pallister-Killian syndrome: tetrasomy of 12pter-->12p11.22 in a boy with an analphoid, inverted duplicated marker chromosomeX-L Huang, M Isabel de Michelena, E Leon, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Genetic Testing|July 14, 2007
The value of MLPA in Waardenburg syndromeJ M Milunsky, T A Maher, M Ito, et al.
American Journal of Medical Genetics|May 9, 2001
Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paragangliomaJ M Milunsky, T A Maher, V V Michels, et al.
Genetic Testing|February 24, 2001
Connexin-26 gene analysis in hearing-impaired newbornsJ M Milunsky, T A Maher, E Yosunkaya, et al.
Clinical Genetics|April 25, 2006
LADD syndrome is caused by FGF10 mutationsJ M Milunsky, G Zhao, T A Maher, et al.
American Journal of Obstetrics and Gynecology|March 1, 1991
Prenatal diagnosis of myotonic muscular dystrophy with linked deoxyribonucleic acid probesA Milunsky, J C Skare, J M Milunsky, et al.
Clinical Genetics|June 7, 2003
XL PCR for the detection of large trinucleotide expansions in juvenile Huntington's diseaseJ M Milunsky, T A Maher, B A Loose, et al.
Clinical Genetics|March 14, 2008
A re-examination of the chromosome 8p22-8p23.1 region in Kabuki syndromeJ M Milunsky, T A Maher, G Zhao, et al.
Prenatal Diagnosis|November 23, 2005
The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysisA Milunsky, C Konialis, S H Shim, et al.
Genetic Testing|April 19, 2002
Mutation analysis in Rett syndromeJ M Milunsky, R V Lebo, T Ikuta, et al.
Clinical Genetics|September 27, 2007
Pallister-Killian syndrome: tetrasomy of 12pter-->12p11.22 in a boy with an analphoid, inverted duplicated marker chromosomeX-L Huang, M Isabel de Michelena, E Leon, et al.
Pageof 2