Mammalian Meiotic Recombination: A Toolbox for Genome Evolution (English)
- New search for: Capilla, Laia
- New search for: Garcia Caldés, Montserrat
- New search for: Ruiz-Herrera, Aurora
- New search for: Capilla, Laia
- New search for: Garcia Caldés, Montserrat
- New search for: Ruiz-Herrera, Aurora
In:
Cytogenetic and Genome Research
;
150
, 1
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1-16
;
2017
- Article (Journal) / Electronic Resource
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Title:Mammalian Meiotic Recombination: A Toolbox for Genome Evolution
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Contributors:
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Published in:Cytogenetic and Genome Research ; 150, 1 ; 1-16
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Publisher:
- New search for: S. Karger AG
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Place of publication:Basel, Switzerland
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Publication date:2017-01-01
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Size:16 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Keywords:
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Source:
Table of contents – Volume 150, 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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Mammalian Meiotic Recombination: A Toolbox for Genome EvolutionCapilla, Laia / Garcia Caldés, Montserrat / Ruiz-Herrera, Aurora et al. | 2017
- 17
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Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp DisomyBragagnolo, Silvia / Colovati, Mileny E.S. / Guilherme, Roberta S. / Dantas, Anelisa G. / de Souza, Malú Zamariolli / de Soares, Maria F. / Melaragno, Maria I. / Perez, Ana B. et al. | 2017
- 23
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2q33.1q34 Deletion in a Girl with Brain Anomalies and Anorectal MalformationRonzoni, Luisa / Novelli, Antonio / Brisighelli, Giulia / Peron, Angela / Triulzi, Fabio / Bianchi, Vera / Leva, Ernesto / Bedeschi, Maria F. et al. | 2017
- 29
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Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(15;19)(q12;p13.3)Dang, Vy / Surampalli, Abhilasha / Manzardo, Ann M. / Youn, Stephanie / Butler, Merlin G. / Gold, June-Anne / Kimonis, Virginia E. et al. | 2017
- 35
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Constitutional Trisomy 8 Mosaicism with Persistent MacrocytosisAltıner, Şule / Kutlay, Nüket Y. / İlhan, Osman et al. | 2017
- 40
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Koolen-de Vries Syndrome: Clinical Report of an Adult and Literature ReviewCiaccio, Claudia / Dordoni, Chiara / Ritelli, Marco / Colombi, Marina et al. | 2017
- 46
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Constitutional Chromoanagenesis of Distal 13q in a Young Adult with Recurrent StrokesBurnside, Rachel D. / Harris, April / Speyer, Darrow / Burgin, W. Scott / Rose, David Z. / Sanchez-Valle, Amarilis et al. | 2017
- 52
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Oncogenic Properties of Candidate Oncogenes in Chromosome Region 17p11.2p12 in Human OsteosarcomaBoth, Joeri / Wu, Thijs / ten Asbroek, Anneloor L.M.A. / Baas, Frank / Hulsebos, Theo J.M. et al. | 2017
- 60
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Aneuploidy Detection and mtDNA Quantification in Bovine Embryos with Different Cleavage Onset Using a Next-Generation Sequencing-Based ProtocolHornak, Miroslav / Kubicek, David / Broz, Petr / Hulinska, Pavlina / Hanzalova, Katerina / Griffin, Darren / Machatkova, Marie / Rubes, Jiri et al. | 2017
- 68
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Occurrence and Origin of Supernumerary Chromosomes in Partamona (Hymenoptera: Apidae: Meliponini)Machado, Diana P. / Miranda, Elder A. / Dessi, Mariana C. / Sabadini, Camila P. / Del Lama, Marco A. et al. | 2017
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Front & Back Matter| 2017