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  1. 1
    The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15.

    The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15. by Thomas Boehm, Richard Baer, Isabelle Lavenir, A. Förster, Jonathan J. Waters, E Nacheva, Terence H. Rabbitts

    Published 1988
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  2. 2
    The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects

    The genetics of folate metabolism and maternal risk of birth of a child with Down syndrome and associated congenital heart defects by Fabio Coppedè

    Published 2015
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  3. 3
    The DNA sequence and comparative analysis of human chromosome 5

    The DNA sequence and comparative analysis of human chromosome 5 by Jeremy Schmutz, Joel Martin, Astrid Terry, Olivier Couronne, Jane Grimwood, Steve Lowry, Laurie Gordon, Duncan Scott, Gary Xie, Wayne Huang, Uffe Hellsten, Mary Bao Tran-Gyamfi, Xinwei She, Shyam Prabhakar, Andrea Aerts, Michael R. Altherr, Eva Bajorek, Stacey Black, Elbert Branscomb, Chenier Caoile, Jean F. Challacombe, Yee Man Chan, Mirian Denys, John C. Detter, Julio Escobar, Dave Flowers, Dea Fotopulos, Tijana Glavina, María Gómez, Eidelyn Gonzales, David Goodstein, Igor V. Grigoriev, Matthew Groza, Nancy Hammon, Trevor Hawkins, Lauren E. Haydu, Sanjay Israni, Jamie Jett, Kristen Kadner, Heather Kimball, Arthur Kobayashi, Frederick Lopez, Yunian Lou, Diego Martinez, Catherine Medina, Jenna Morgan, Richard D. Nandkeshwar, James P. Noonan, Sam Pitluck, Martin Pollard, Paul Predki, James R. Priest, Lucı́a Ramı́rez, James Retterer, Álex Rodríguez, Stephanie Rogers, Asaf Salamov, Angelica Salazar, Nina Thayer, Hope Tice, Ming Jer Tsai, Anna Ustaszewska, Nu Vo, Jeremy Wheeler, Kevin Wu, Joan Yang, Mark Dickson, Jan‐Fang Cheng, Evan E. Eichler, Anne Olsen, L Pennacchio, Daniel S. Rokhsar, Paul Richardson, Susan Lucas, R Myers, Edward M. Rubin

    Published 2004
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  4. 4
    Synaptophysin and Synaptojanin-1 in Down Syndrome are Differentially Affected by Alzheimer's Disease

    Synaptophysin and Synaptojanin-1 in Down Syndrome are Differentially Affected by Alzheimer's Disease by Sarah B. Martin, Amy L.S. Dowling, Joann Lianekhammy, Ira T. Lott, Eric Doran, M. Paul Murphy, Tina L. Beckett, Frederick A. Schmitt, Elizabeth Head

    Published 2014
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  5. 5
    DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies

    DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies by Jianling Ji, Hane Lee, Bob Argiropoulos, Naghmeh Dorrani, John Mann, Julián A. Martínez-Agosto, Natalia Gomez‐Ospina, Natalie M. Gallant, Jonathan A. Bernstein, Louanne Hudgins, Leah Slattery, Bertrand Isidor, Cédric Le Caignec, Albert David, Ewa Obersztyn, Barbara Wiśniowiecka‐Kowalnik, Michelle Fox, Joshua L. Deignan, Éric Vilain, Emily Hendricks, Margaret Harr, Sarah E. Noon, Jessi R Jackson, Alisha Wilkens, Ghayda Mirzaa, Noriko Salamon, Jeff Abramson, Elaine H. Zackai, Ian D. Krantz, A. Micheil Innes, Stanley F. Nelson, Wayne W. Grody, Fabiola Quintero‐Rivera

    Published 2015
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  6. 6
    Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation

    Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation by Jennifer A. Scott, Sharon L. Wenger, Mark W. Steele, Aravinda Chakravarti

    Published 1995
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  7. 7
    Self-Organizing Feature Maps Identify Proteins Critical to Learning in a Mouse Model of Down Syndrome

    Self-Organizing Feature Maps Identify Proteins Critical to Learning in a Mouse Model of Down Syndrome by Clara Higuera, Katheleen Gardiner, Krzysztof J. Cios

    Published 2015
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  8. 8
    The role of DYRK1A in neurodegenerative diseases

    The role of DYRK1A in neurodegenerative diseases by Jerzy Węgiel, Cheng‐Xin Gong, Yu‐Wen Hwang

    Published 2010
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  9. 9
    Physical and genetic mapping of Candida albicans: several genes previously assigned to chromosome 1 map to chromosome R, the rDNA-containing linkage group

    Physical and genetic mapping of Candida albicans: several genes previously assigned to chromosome 1 map to chromosome R, the rDNA-containing linkage group by Brian L. Wickes, Jeff L. Staudinger, B B Magee, Kyung J. Kwon‐Chung, P. T. Magee, Stephen W. Scherer

    Published 1991
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  10. 10
    Induced chromosome deletions cause hypersociability and other features of Williams–Beuren syndrome in mice

    Induced chromosome deletions cause hypersociability and other features of Williams–Beuren syndrome in mice by Hong Hua Li, Madhuri Roy, Unsal Kusçuoglu, Corinne M. Spencer, Birgit Halm, Katharine C. Harrison, J. Henri Bayle, Alessandra Splendore, Feng Ding, Leslie Meltzer, Elena Wright, Richard Paylor, Karl Deisseroth, Uta Francke

    Published 2009
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  11. 11
    LINKAGE RELATIONSHIPS OF 19 ENZYME LOCI IN MAIZE

    LINKAGE RELATIONSHIPS OF 19 ENZYME LOCI IN MAIZE by M. M. Goodman, C. W. Stuber, Kathleen J. Newton, H. Weissinger

    Published 1980
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  12. 12
    A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome

    A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome by Frances K. Wiseman, Tamara Al‐Janabi, John Hardy, Annette Karmiloff‐Smith, Dean Nižetić, Victor L. J. Tybulewicz, Elizabeth Fisher, André Strydom

    Published 2015
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  13. 13
    Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21

    Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21 by Chi-Ming Li, Meirong Guo, Martha Salas, Nicole Schupf, Wayne Silverman, Warren B. Zigman, Sameera Husain, Dorothy Warburton, Harshwardhan M. Thaker, Benjamin Tycko

    Published 2006
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  14. 14
    A RAPID CHROMOSOME-MAPPING METHOD FOR CLONED FRAGMENTS OF YEAST DNA

    A RAPID CHROMOSOME-MAPPING METHOD FOR CLONED FRAGMENTS OF YEAST DNA by S. Carl Falco, David Botstein

    Published 1983
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  15. 15
    A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross.

    A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross. by Monica J. Justice, Linda D. Siracusa, Debra J. Gilbert, Nora Heisterkamp, John Groffen, Kiran Chada, Colleen M. Silan, N G Copeland, N A Jenkins

    Published 1990
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  16. 16
    <i>App</i>Gene Dosage Modulates Endosomal Abnormalities of Alzheimer's Disease in a Segmental Trisomy 16 Mouse Model of Down Syndrome

    <i>App</i>Gene Dosage Modulates Endosomal Abnormalities of Alzheimer's Disease in a Segmental Trisomy 16 Mouse Model of Down Syndrome by Anne M. Cataldo, Suzana Petanceska, Corrinne M. Peterhoff, Nicole B. Terio, Charles J. Epstein, Angela J. Villar, Elaine J. Carlson, Matthias Staufenbiel, Ralph A. Nixon

    Published 2003
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  17. 17
    Structure, Organization, and Sequence of Alpha Satellite DNA from Human Chromosome 17: Evidence for Evolution by Unequal Crossing-Over and an Ancestral Pentamer Repeat Shared With the Human X Chromosome

    Structure, Organization, and Sequence of Alpha Satellite DNA from Human Chromosome 17: Evidence for Evolution by Unequal Crossing-Over and an Ancestral Pentamer Repeat Shared With... by John S. Waye, Huntington F. Willard

    Published 1986
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  18. 18
    Down Syndrome Cognitive Phenotypes Modeled in Mice Trisomic for All HSA 21 Homologues

    Down Syndrome Cognitive Phenotypes Modeled in Mice Trisomic for All HSA 21 Homologues by Pavel V. Belichenko, Alexander M. Kleschevnikov, Ann Becker, Grant E. Wagner, Larisa V. Lysenko, Yichao Yu, William C. Mobley

    Published 2015
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  19. 19
    The (6;9) chromosome translocation, associated with a specific subtype of acute nonlymphocytic leukemia, leads to aberrant transcription of a target gene on 9q34.

    The (6;9) chromosome translocation, associated with a specific subtype of acute nonlymphocytic leukemia, leads to aberrant transcription of a target gene on 9q34. by Marieke von Lindern, Annemarie Poustka, H Lerach, Gerard C. Grosveld

    Published 1990
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  20. 20
    Acute myeloid leukemia with the 8q22;21q22 translocation: secondary mutational events and alternative t(8;21) transcripts

    Acute myeloid leukemia with the 8q22;21q22 translocation: secondary mutational events and alternative t(8;21) transcripts by Luke F. Peterson, Anita Boyapati, E. Ahn, Joseph R. Biggs, Akiko Okumura, Miao‐Chia Lo, Ming Yan, Dong‐Er Zhang

    Published 2007
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