Lack of founding Amerindian mitochondrial DNA lineages in extinct Aborigines from Tierra del Fuego-Patagonia (English)
- New search for: Lalueza, C.
- New search for: Perez-Perez, A.
- New search for: Prats, E.
- New search for: Cornudella, L.
- New search for: Turbon, D.
- New search for: Lalueza, C.
- New search for: Perez-Perez, A.
- New search for: Prats, E.
- New search for: Cornudella, L.
- New search for: Turbon, D.
In:
HUMAN MOLECULAR GENETICS
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6
, 1
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41-46
;
1997
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ISSN:
- Article (Journal) / Print
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Title:Lack of founding Amerindian mitochondrial DNA lineages in extinct Aborigines from Tierra del Fuego-Patagonia
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Contributors:Lalueza, C. ( author ) / Perez-Perez, A. ( author ) / Prats, E. ( author ) / Cornudella, L. ( author ) / Turbon, D. ( author )
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Published in:HUMAN MOLECULAR GENETICS ; 6, 1 ; 41-46
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Publisher:
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Publication date:1997-01-01
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Size:6 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 572.8
- Further information on Dewey Decimal Classification
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Classification:
DDC: 572.8 -
Source:
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Table of contents – Volume 6, Issue 1
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1
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The IL-9 Receptor Gene, Located in the Xq/Yq Pseudoautosomal Region, Has an Autosomal Origin, Escapes X Inactivation and Is Expressed from the YVermeesch, Joris Robert / Petit, Paul / Kermouni, Abdenaïm / Renauld, Jean-Christophe / Van Den Berghe, Herman / Marynen, Peter et al. | 1997
- 9
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Emergence and Scattering of Multiple Neurofibromatosis (NF1)-Related Sequences During Hominoid Evolution Suggest a Process of Pericentromeric Interchromosomal TranspositionRégnier, Vinciane / Meddeb, Mounira / Lecointre, Guillaume / Richard, Florence / Duverger, Annette / Van Cong, Nguyen / Dutrillaux, Bernard / Bernheim, Alain / Danglot, Gisèle et al. | 1997
- 17
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Mutations in the Gene Encoding the Inwardly-Rectifying Renal Potassium Channel, ROMK, Cause the Antenatal Variant of Bartter Syndrome: Evidence for Genetic HeterogeneityKárolyi, Lothar / Konrad, Martin / Köckerling, Arnold / Ziegler, Andreas / Zimmermann, Dorthe K. / Roth, Bernd / Wieg, Christian / Grzeschik, Karl-Heinz / Koch, Manuela C. / Seyberth, Hannsjörg W. et al. | 1997
- 27
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A Newly Identified Locus for Usher Syndrome Type I, USH1E, Maps to Chromosome 21q21Chaïb, Hassan / Kaplan, Josseline / Gerber, Sylvie / Vincent, Christophe / Ayadi, Hammadi / Slim, Rima / Munnich, Arnold / Weissenbach, Jean / Petit, Christine et al. | 1997
- 33
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Translation Initiation Factor eIF-4gamma is Encoded by an Amplified Gene and Induces an Immune Response in Squamous Cell Lung CarcinomaBrass, Nicole / Heckel, Dirk / Sahin, Ugor / Pfreundschuh, Michael / Sybrecht, Gerhard W. / Meese, Eckart et al. | 1997
- 41
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Lack of Founding Amerindian Mitochondrial DNA Lineages in Extinct Aborigines from Tierra del Fuego-PatagoniaLalueza, Carles / Pérez-Pérez, Alejandro / Prats, Eva / Cornudella, Lluís / Turbón, Daniel et al. | 1997
- 47
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A Locus for Autosomal Dominant Posterior Polar Cataract on Chromosome 1pIonides, Alexander C. W. / Berry, Vanita / Mackay, Donna S. / Moore, Anthony T. / Bhattacharya, Shomi S. / Shiels, Alan et al. | 1997
- 53
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The BRC Repeats are Conserved in Mammalian BRCA2 ProteinsBignell, Graham / Micklem, Gos / Stratton, Michael R. / Ashworth, Alan / Wooster, Richard et al. | 1997
- 59
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Functional Human CFTR Produced by Stable Chinese Hamster Ovary Cell Lines Derived Using Yeast Artificial ChromosomesMogayzel, Peter J. / Henning, Karla A. / Bittner, Michael L. / Novotny, Elizabeth A. / Schwiebert, Erik M. / Guggino, William B. / Jiang, Yuan / Rosenfeld, Melissa A. et al. | 1997
- 69
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Comparison of the Human and Mouse Genes Encoding the Telomeric Protein, TRF1: Chromosomal Localization, Expression and Conserved Protein DomainsBroccoli, Dominique / Chong, Laura / Oelmann, Stefan / Fernald, Anthony A. / Marziliano, Nicola / van Steensel, Bas / Kipling, David / Le Beau, Michelle M. / de Lange, Titia et al. | 1997
- 77
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Trinucleotide Repeats in the Human Genome: Size Distributions for All Possible Triplets and Detection of Expanded Disease Alleles in a Group of Huntington Disease Individuals by the Repeat Expansion Detection MethodHofferbert, Sigrun / Schanen, N. Carolyn / Chehab, Farid / Francke, Uta et al. | 1997
- 85
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Increased Proportion of Exon 9 Alternatively Spliced CFTR Transcripts in vas Deferens Compared with Nasal Epithelial CellsTeng, Hui / Jorissen, Mark / Van Poppe, Hein / Legius, Eric / Cassiman, Jean-Jacques / Cuppens, Harry et al. | 1997
- 91
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Mutational Analysis of the SOX9 Gene in Campomelic Dysplasia and Autosomal Sex Reversal: Lack of Genotype/Phenotype CorrelationsMeyer, Jobst / Südbeck, Peter / Held, Marika / Wagner, Thomas / Schmitz, M. Lienhard / Dagna Bricarelli, Franca / Eggermont, Ephrem / Friedrich, Ursula / Haas, Oskar A. / Kobelt, Albrecht et al. | 1997
- 99
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Quantification, by Solid-Phase Minisequencing, of the Telomeric and Centromeric Copies of the Survival Motor Neuron Gene in Families with Spinal Muscular AtrophySchwartz, Marianne / Sørensen, Nicolina / Hansen, Flemming Juul / Hertz, Jens Michael / Nørby, Søren / Tranebjærg, Lisbeth / Skovby, Flemming et al. | 1997
- 105
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Cancer Risk Associated with Germline DNA Mismatch Repair Gene MutationsDunlop, Malcolm G. / Farrington, Susan M. / Carothers, Andrew D. / Wyllie, Andrew H. / Sharp, Linda / Burn, John / Liu, Bo / Kinzler, Kenneth W. / Vogelstein, Bert et al. | 1997
- 111
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Myosin VIIA Gene: Heterogeneity of the Mutations Responsible for Usher Syndrome Type IBLévy, Gallia / Levi-Acobas, Fabienne / Blanchard, Stéphane / Gerber, Sylvie / Larget-Piet, Dominique / Chenal, Viviane / Liu, Xue-Zhong / Newton, Valerie / Steel, Karen P. / Brown, Steve D. M. et al. | 1997
- 117
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Identification of a Complex Congenital Heart Defect Susceptibility Locus by Using DNA Pooling and Shared Segment AnalysisSheffield, Val C. / Pierpont, Mary Ella / Nishimura, Darryl / Beck, John S. / Burns, Trudy L. / Berg, Mary Anne / Stone, Edwin M. / Patil, Shivanand R. / Lauer, Ronald M. et al. | 1997
- 123
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Localization of a Gene for Oculodentodigital Syndrome to Human Chromosome 6q22-q24Gladwin, Amanda / Donnai, Dian / Metcalfe, Kay / Schrander-Stumpel, Connie / Brueton, Louise / Verloes, Alain / Aylsworth, Arthur / Toriello, Helga / Winter, Robin / Dixon, Michael et al. | 1997
- 129
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Somatic Mutation Processes at a Muman MinisatelliteJeffreys, Alec J. / Neumann, Rita et al. | 1997
- 129
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Somatic mutation processes at a human minisatelliteJeffreys, A. J. / Neumann, R. et al. | 1997
- 137
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Genotype-Phenotype Correlation for Nucleotide Substitutions in the IgII-IgIII Linker of FGFR2Oldridge, Michael / Lunt, Peter W. / Zackai, Elaine H. / McDonald-McGinn, Donna M. / Muenke, Maximilian / Moloney, Dominique M. / Twigg, Stephen R. F. / Heath, John K. / Howard, Timothy D. / Hoganson, George et al. | 1997