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Results 11-20 of 21 (Search time: 0.004 seconds).
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Isodicentric Y chromosomes and secondary microchromosomes.
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Prevalence of the BCR/ABL1 transcripts in Mexican patients with chronic myelogenous leukemia
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MLH1 and XRCC1 polymorphisms in Mexican patients with colorectal cancer
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XRCC1 polymorphisms and haplotypes in Mexican patients with acute lymphoblastic leukemia
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46,XX ovotesticular disorder in a Mexican patient with Beckwith–Wiedemann syndrome: a case report.
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Increased expression of AML1-a and acquired chromosomal abnormalities in childhood acute lymphoblastic leukemia
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True vs. false inv(Y)(p11q11.2): a familial instance concurrent with trisomy 21
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Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia.
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A 45,X sterile male with Yp disguised as 21p
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A de novo interstitial 6q deletion in a boy with a split hand malformation
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Descubre
Author
9
Meza Espinoza, Juan Pablo
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Rivera, Horacio
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González García, Juan Ramón
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Ayala Madrigal, María de la Luz
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Barros Núñez, Patricio
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Leal Ugarte, Evelia
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Macías Gómez, Nelly
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Peralta Leal, Valeria
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Esparza Flores, María Amparo
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Picos Cárdenas, Verónica Judith
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Subject
1
21 translocations
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21q proximal tetrasomy
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3p deletion syndrome
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3p- syndrome
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45,X males
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acquired chromosomal abnormalities
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AML1-a isoform
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array-CGH analysis
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autosome translocations
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b2a2 and b3a2 transcripts
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