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Results: 1-3 |
Results: 3
Genetic mapping of autosomal dominant charcot-marie-tooth disease in a large french-acadian kindred; identification of new linked markers on chromosome 17
Authors: Patel, Pragna I. Franco, Brunella Garcia, Carlos Slaugenhaupt, Susan A. Nakamura, Yusuke Ledbetter, David H. Chakravarti, Aravinda Lupski, James R.
Citation: I. Patel, Pragna et al., Genetic mapping of autosomal dominant charcot-marie-tooth disease in a large french-acadian kindred; identification of new linked markers on chromosome 17, American journal of human genetics , 46-II(4), 1990, pp. 801-809
Mutations of the Mitochondrial Holocytochrome c.Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome
Authors: Wimplinger, Isabella Morleo, Manuela Rosenberger, Georg Iaconis, Daniela Orth, Ulrike Meinecke, Peter Lerer, Israela Ballabio, Andrea Gal, Andreas Franco, Brunella Kutsche, Kerstin
Citation: Wimplinger, Isabella et al., Mutations of the Mitochondrial Holocytochrome c.Type Synthase in X-Linked Dominant Microphthalmia with Linear Skin Defects Syndrome, American journal of human genetics , 79(5), 2006, pp. 878-889
Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids.
Authors: Patel, Pragna I. Garcia, Carlos Montes de Oca-Luna, Roberto Malamut, Richard I. Franco, Brunella Slaugenhaupt, Susan Chakravarti, Aravinda Lupski, James R.
Citation: I. Patel, Pragna et al., Isolation of a marker linked to the Charcot-Marie-Tooth disease type IA gene by differential Alu-PCR of human chromosome 17-retaining hybrids., American journal of human genetics , 47-II(6), 1990, pp. 926-934
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