-
1
المؤلفون: Angela J. Marlow, Anthony Cox, Andrew Pickles, Patrick Bolton, Elaine Thompson, Lisa Chrzanowski, Pat Scudder, Kim S. Beyer, Jeanne Fremolle-Kruck, Ros Packer, Anthony P. Monaco, Annemarie Poustka, Janine Michelotti, Axel Benner, Karen Brøndum-Nielsen, Michael Rutter, Christina Corsello, Elizabeth P. Green, Tom Berney, Jane Whittacker, Fred R. Volkmar, Bennett L. Leventhal, Catherine Wainhouse, Simon Wallace, Maretha de Jonge, Elena Maestrini, Sabine M. Klauck, Claire Garner, Catherine Pienkowski, Ramyani Gupta, Alina Paul, David L. Pauls, Chantal Kemner, Edwin H. Cook, Katerina Papanikolaou, Marie Thérèse Tauber, Eric Fombonne, Pamela Warburton, Catherine Lord, Lennart Pedersen, Jonathan Green, Thomas Kelly, Amaia Hervas, Bernadette Rogé, Helen McConachie, Sabine Feineis-Matthews, Sabine Epp, Gillian Baird, Anne Aubin, Rodney M. J. Cotterill, Fritz Poustka, Janette Moore, Amy Liu, Martha Turner, Daniel E. Weeks, Janine A. Lamb, Julia Bailey, Martha Dedricks, John Tsiantis, Sven Bölte, Jennifer G. Levitt, Sarah Palferman, Gabriele Schmötzer, Nicola Matthews, Zoe Docherty, Gabrielle Barnby, Stephen Abbs, Susan L. Smalley, Bryan Bolton, Ann Le Couteur, Marianne Murin, Herman van Engeland, Dorothea Rühl, Petrus J. de Vries, Stephen J. Guter, Anthony J. Bailey, Demetrious Haracopos, Gunna Eriksen, Anne Gilchrist
المصدر: ResearcherID
مصطلحات موضوعية: Genetic Markers, Male, Linkage disequilibrium, Genotype, Genetic Linkage, Biology, Polymerase Chain Reaction, Neurodevelopmental disorder, Genetic linkage, Genetics, medicine, Genetic predisposition, Chromosomes, Human, Humans, Allele, Autistic Disorder, Molecular Biology, Genetics (clinical), Alleles, Linkage (software), Linkage Disequilibrium Mapping, Chromosome Mapping, General Medicine, medicine.disease, Genetic marker, Female, Disease Susceptibility, Chromosomes, Human, Pair 7
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9330fb92598bb1503b0d3a73b77d092
https://ora.ox.ac.uk/objects/uuid:8de04b5a-0fd5-41d3-8f2e-0319b44f97aa -
2
المؤلفون: Julian Barwell, Susan Bint, Pamela Warburton, Miranda Splitt, Caroline Mackie Ogilvie, Darryl J. Maxwell
المصدر: European Journal of Human Genetics. 11:749-753
مصطلحات موضوعية: Adult, Male, Neocentromere, Derivative chromosome, Marker chromosome, Centromere, Ring chromosome, Mitosis, Biology, Chromosome 16, Pregnancy, Prenatal Diagnosis, Genetics, Humans, Ring Chromosomes, Fetal Death, In Situ Hybridization, In Situ Hybridization, Fluorescence, Genetics (clinical), Chromosome Aberrations, Telomere, Molecular biology, Chromosome Banding, Phenotype, Chromosome 4, Karyotyping, Female, Chromosomes, Human, Pair 4, Chromosome 21, Chromosome 22, Cell Division, Gene Deletion
-
3
المؤلفون: Brian W. Jacobs, Kathleen Morris, Zoe Docherty, Shirley Hodgson, Pamela Warburton, Gillian Baird, Wai Chen
المصدر: American Journal of Medical Genetics. 96:228-234
مصطلحات موضوعية: Male, Genetic Linkage, Specific language impairment, Biology, Translocation, Genetic, Genetic determinism, medicine, Humans, Heritability of autism, Language disorder, Autistic Disorder, Child, In Situ Hybridization, Fluorescence, Genetics (clinical), Chromosome 7 (human), Genetics, Language Disorders, Infant, medicine.disease, Twin study, Chromosome Banding, Pedigree, Developmental disorder, Phenotype, Child, Preschool, Karyotyping, Autism, Female, Chromosomes, Human, Pair 7
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c86cace4a860b8eef61071c9f990449
https://doi.org/10.1002/(sici)1096-8628(20000403)96:2<228::aid-ajmg20>3.0.co;2-g -
4
المؤلفون: Caroline Mackie Ogilvie, Pamela Warburton, Shehla Mohammed
المصدر: American Journal of Medical Genetics. 91:51-55
مصطلحات موضوعية: Family Health, Male, Genetics, Adolescent, Derivative chromosome, Karyotype, Chromosomal translocation, Telomere, Biology, Subtelomere, medicine.disease, Translocation, Genetic, Genetic determinism, Pedigree, Developmental disorder, Chromosomes, Human, Pair 1, Karyotyping, medicine, Humans, Fish
, Female, Abnormality, Chromosomes, Human, Pair 16, In Situ Hybridization, Fluorescence, Genetics (clinical) URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddd6d88159d9b4a855df0b2403a4b420
https://doi.org/10.1002/(sici)1096-8628(20000306)91:1<51::aid-ajmg9>3.0.co;2-h -
5
المؤلفون: Elizabeth P. Green, David Pauls, Katerina Papanikolaou, Amaia Hervas, Alina Paul, De, Vries, Pj, Lennart Pedersen, Axel Benner, Catherine Lord, Fred R. Volkmar, Sabine Feineis-Matthews, Jennifer G. Levitt, Angela J. Marlow, Helen McConachie, Emily J. Thompson, Claire Garner, Catherine Pienkowski, Janette Moore, Gabriele Schmötzer, Nicola Matthews, Nuala Ryder, Anne Gilchrist, De, Jonge, Mv, Van, Engeland, H, Anne Aubin, Christine M. Freitag, Stephen Abbs, Ros Packer, Catherine Wainhouse, Antony Cox, KB Nielsen, Susan L. Smalley, Daniel E. Weeks, Bryan Bolton, Eric Fombonne, S Boolte, Francesca Blasi, Sabine M. Klauck, Rmj Cotterill, Andrew Pickles, Kim S. Beyer, Gillian Baird, Annemarie Poustka, Marianne Murin, Christina Corsello, Int, Mol, Genetic, Study, Autism, Cons, Elena Maestrini, Simon Wallace, Anthony P. Monaco, Julia Bailey, Janine Michelotti, Thomas Kelly, Le, Couteur, A, Stephen J. Guter, Anthony J. Bailey, B Rogee, Sarah Palferman, Demetrious Haracopos, Gunna Eriksen, James J. McGough, Zoe Docherty, Maïté Tauber, E Cottington, Patrick Bolton, Martha Turner, Fritz Poustka, Jeanne Fremolle-Kruck, Gabrielle Barnby, Dorothea Rühl, John Tsiantis, Pat Scudder, Bennett L. Leventhal, T Berney, Michael Rutter, Jeremy R. Parr, Edwin H. Cook, Pamela Warburton, Chantal Kemner, Jane Whittacker, Ramyani Gupta, Sabine Epp, JW Goethe, Jonathan Green, Janine A. Lamb
المصدر: ResearcherID
مصطلحات موضوعية: Molecular Sequence Data, Biology, 03 medical and health sciences, 0302 clinical medicine, Chromosome 16, Genetics, medicine, Humans, Heritability of autism, Genetic Predisposition to Disease, Genetic Testing, Allele, Autistic Disorder, Genetics (clinical), X chromosome, Alleles, 030304 developmental biology, Chromosome 7 (human), 0303 health sciences, Chromosome, Articles, medicine.disease, Chromosome 17 (human), Chromosomes, Human, Pair 2, Autism, 030217 neurology & neurosurgery, Chromosomes, Human, Pair 16, Chromosomes, Human, Pair 7
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcf34322e3855df0fcd67fdd968afc76
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000170271400009&KeyUID=WOS:000170271400009