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by Ballantyne, Kaye and Ralf, Arwin and Aboukhalid, Rachid and Achakzai, Niaz and Anjos, Tania and Ayub, Qasim and Balažic, Jože and Ballantyne, Jack and Ballard, David and Berger, Burkhard and Bobillo, Cecilia and Bouabdellah, Mehdi and Burri, Helen and Capal, Tomas and Caratti, Stefano and Cárdenas, Jorge and Cartault, François and Carvalho, Elizeu and Carvalho, Margarete and Cheng, Baowen and Coble, Michael and Comas, David and Corach, Daniel and D'Amato, Mauro and Davison, Sean and Knijff, Peter and Ungria, Maria Corazon and Decorte, Ronny and Dobosz, Tadeusz and Dupuy, Berit and Elmrghni, Samir and Gliwiński, Mateusz and Gomes, Sara and Grol, Laurens and Haas, Cordula and Hanson, Erin and Henke, Jürgen and Henke, Lotte and Herrera-Roíguez, Fabiola and Hill, Carolyn and Holmlund, Gunilla and Honda, Katsuya and Immel, Uta-Dorothee and Inokuchi, Shota and Jobling, R and Kaddura, Mahmoud and Kim, Jong and Kim, Soon and Kim, Wook and King, Turi and Klausriegler, Eva and Kling, Daniel and Kovačević, Lejla and Kovatsi, Leda and Krajewski, Paweł and Kravchenko, Sergey and Larmuseau, Maarten and Lee, Eun Young and Lessig, Rüdiger and Livshits, Ludmila and Marjanović, Damir and Minarik, Marek and Mizuno, Natsuko and Moreira, Helena and Morling, Niels and Mukherjee, Meeta and Munier, Patrick and Nagaraju, Javaregowda and Neuhuber, Franz and Nie, Shengjie and Nilasitsataporn, Premlaphat and Nishi, Takeki and Oh, Hye and Olofsson, Sylvia and Onofri, Valerio and Palo, Jukka and Pamjav, Horolma and Parson, Walther and Petlach, Michal and Phillips, Christopher and Ploski, Rafal and Prasad, Samayamantri P and Primorac, gan and Purnomo, Gludhug and Purps, Josephine and Rangel-Villalobos, Hector and Reogonekbała, Krzysztof and Rerkamnuaychoke, Budsaba and Gonzalez, Danel Rey and Robino, Carlo and Roewer, Lutz and Rosa, Anna and Sajantila, Antti and Sala, Anea and Salvador, Jazelyn and Sanz, Paula and Schmitt, Christian and Sharma, Anisha K and Silva, Dayse and Shin, Kyoung-Jin and ... and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Hälsouniversitetet and Avdelningen för mikrobiologi och molekylär medicin
Human Mutation, ISSN 1059-7794, 01/2014, Volume 35, Issue 8, pp. 1021 - 1032
Journal Article
2007, ISBN 9789812703743, viii, 314
Book
03/2011
Introduction: The application of Y-Chromosome molecular DNA typing is a tool of recognized importance in the process of identification of male individuals in... 
Colombia | STR-Y | Cromosoma-Y | Haplotype diversity | Haplotipo | Y-Chromosome | Diversidad haplotípica | Haplotype
Web Resource
Estudio de alteraciones cromosómicas y su relación con el crecimiento in vitro en células de meningiomas (Chromosomal alterations of meningioma cells and its relation to growth in vitro), 12/2006
Objectives: To demonstrate the frequency of chromosomic alterations and their relationship to the growth velocity of in vitro meningioma cells cultures. Data... 
Cultivo in vitro de células tumorales | In vitro tumoral cell culture | Chromosomes | Meningioma | Meningiomas | Cromosomas
Journal
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 7341 - 13
Haplogroup R1b-M269 comprises most Western European Y chromosomes; of its main branches, R1b-DF27 is by far the least known, and it appears to be highly... 
EUROPE | POPULATION-GENETICS | LANDSCAPE | MULTIDISCIPLINARY SCIENCES | EXPANSION | FREQUENCY | STR LOCI | DIVERSITY | DEMOGRAPHY | HISTORY | SPAIN | Short tandem repeats | Y Chromosomes | Age | Cromosoma Y | Genòmica
Journal Article
Revista de Ciencias Médicas de Pinar del Río, 06/2017, Volume 21, Issue 4, pp. 571 - 597
Introduction: Ehlers-Danlos syndrome is a rare disease which diagnosis is in many cases underestimated. It is an inherited disease, caused by chromosomal... 
TEJIDO CONECTIVO | FIBROMIALGIA | INESTABILIDAD DE LA ARTICULACIÓN | SÍNDROME DE EHLERS-DANLOS | CROMOSOMA X
Journal Article
2012, Chicago studies in practices of meaning, ISBN 9780226201405, cm.
"The Genealogical Science" analyzes the scientific work and social implications of the flourishing field of genetic history. A biological discipline that... 
Jews | Jews-Identity | Genetics | Y chromosome | Cohanim | Identity
Book
Anales de pediatria (Barcelona, Spain : 2003), ISSN 1695-4033, 01/2015, Volume 82, Issue 1, pp. e189 - e191
ATR-16 syndrome is due to alterations on chromosome 16p13.3, and is usually accompanied by alpha-thalassemia, mild-moderate mental retardation, dysmorphic... 
ATR-16 syndrome | Síndrome ATR-16 | Chromosome 16p | Osteosarcoma | Cromosoma 16p
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2013, Volume 8, Issue 5, p. e65441
Journal Article
16.