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1
09/15: Comparative Genomics of a Conserved Chromosomal Region Associated with a Complex Human Phenotype
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09/15: Comparative Genomics of a Conserved Chromosomal Region Associated with a Complex Human Phenotype

Kappen, Claudia ; Salbaum, J.Michael

Genomics (San Diego, Calif.), 2001-04, Vol.73 (2), p.171-178 [Peer Reviewed Journal]

San Diego, CA: Elsevier Inc

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2
1, 2, 3: Counting the fingers on a chicken wing
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1, 2, 3: Counting the fingers on a chicken wing

Carkett, Martin D ; Logan, Malcolm PO

Genome biology, 2011-01, Vol.12 (10), p.130-130 [Peer Reviewed Journal]

England: Springer-Verlag

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3
1,000-loci transcript map of the barley genome: new anchoring points for integrative grass genomics
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1,000-loci transcript map of the barley genome: new anchoring points for integrative grass genomics

Stein, Nils ; Prasad, Manoj ; Scholz, Uwe ; Thiel, Thomas ; Zhang, Hangning ; Wolf, Markus ; Kota, Raja ; Varshney, Rajeev K ; Perovic, Dragan ; Grosse, Ivo ; Graner, Andreas

Theoretical and applied genetics, 2007-03, Vol.114 (5), p.823-839 [Peer Reviewed Journal]

Heidelberg: Berlin/Heidelberg : Springer-Verlag

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4
1+1 = 3: a fusion of 2 enzymes in the methionine salvage pathway of Tetrahymena thermophila creates a trifunctional enzyme that catalyzes 3 steps in the pathway
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1+1 = 3: a fusion of 2 enzymes in the methionine salvage pathway of Tetrahymena thermophila creates a trifunctional enzyme that catalyzes 3 steps in the pathway

Salim, Hannah M W ; Negritto, Maria Cristina ; Cavalcanti, Andre R O Dutcher, Susan K.

PLoS genetics, 2009-10, Vol.5 (10), p.e1000701-e1000701 [Peer Reviewed Journal]

United States: Public Library of Science

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5
1.15 Mb microdeletion in chromosome band 20p13 associated with moderate developmental delay—Additional case and data's review
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1.15 Mb microdeletion in chromosome band 20p13 associated with moderate developmental delay—Additional case and data's review

Jezela‐Stanek, Aleksandra ; Kucharczyk, Marzena ; Pelc, Magdalena ; Gutkowska, Anna ; Krajewska‐Walasek, Małgorzata

American journal of medical genetics. Part A, 2013-01, Vol.161 (1), p.172-178 [Peer Reviewed Journal]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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6
1,2-Dibromo-3-chloropropane (DBCP) is positive for sex-linked recessive lethals, heritable translocations and chromosome loss in Drosophila
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1,2-Dibromo-3-chloropropane (DBCP) is positive for sex-linked recessive lethals, heritable translocations and chromosome loss in Drosophila

Zimmering, S.

Mutation research, 1983-01, Vol.119 (3), p.287-288 [Peer Reviewed Journal]

Netherlands: Elsevier B.V

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7
1,2-dimethylhydrazine carcinogenesis in C3HA and CBA female mice prenatally treated with diethylstilbestrol
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1,2-dimethylhydrazine carcinogenesis in C3HA and CBA female mice prenatally treated with diethylstilbestrol

Turusov, Vladimir S. ; Trukhanova, Lyubov S. ; Lanko, Natalya S. ; Morozova, Olga V. ; Gorbacheva, Elena V. ; Politova, Sophia N.

Teratogenesis, carcinogenesis, and mutagenesis, 1997, Vol.17 (1), p.19-28

New York: Wiley Subscription Services, Inc., A Wiley Company

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8
1,2:3,4-Diepoxybutane Induces Multipolar Mitosis in Cultured Human Lymphocytes
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1,2:3,4-Diepoxybutane Induces Multipolar Mitosis in Cultured Human Lymphocytes

Barajas Torres, Reyna Lucía ; Domínguez Cruz, Martín Daniel ; Borjas Gutiérrez, César ; Ramírez Dueñas, María de Lourdes ; Magaña Torres, María Teresa ; González García, Juan Ramón

Cytogenetic and genome research, 2016-01, Vol.148 (2-3), p.179-184 [Peer Reviewed Journal]

Basel, Switzerland

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9
A 0.5-Mbp deletion on bovine chromosome 23 is a strong candidate for stillbirth in Nordic Red cattle
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A 0.5-Mbp deletion on bovine chromosome 23 is a strong candidate for stillbirth in Nordic Red cattle

Sahana, Goutam ; Iso-Touru, Terhi ; Wu, Xiaoping ; Nielsen, Ulrik Sander ; de Koning, Dirk-Jan ; Lund, Mogens Sandø ; Vilkki, Johanna ; Guldbrandtsen, Bernt

Genetics selection evolution (Paris), 2016-04, Vol.48 (1), p.35-35, Article 35 [Peer Reviewed Journal]

France: BioMed Central

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10
A 0.7 Mb de novo duplication at 7q21.3 including the genes DLX5 and DLX6 in a patient with split‐hand/split‐foot malformation
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A 0.7 Mb de novo duplication at 7q21.3 including the genes DLX5 and DLX6 in a patient with split‐hand/split‐foot malformation

Velinov, Milen ; Ahmad, Ausaf ; Brown‐Kipphut, Brigette ; Shafiq, Mustafa ; Blau, Jonathan ; Cooma, Ruby ; Roth, Philip ; Iqbal, M. Anwar

American journal of medical genetics. Part A, 2012-12, Vol.158A (12), p.3201-3206 [Peer Reviewed Journal]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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