Biselli, J M <br/><br/>
Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.  [electronic resource] 

 -  Genetic counseling (Geneva, Switzerland)  2009 
 - 225-34 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1015-8146 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Alleles<br/>Aneuploidy<br/>Brazil<br/>Chromosomes, Human, X--genetics<br/>Chromosomes, Human, Y--genetics<br/>DNA Mutational Analysis<br/>Down Syndrome--diagnosis<br/>Female<br/>Ferredoxin-NADP Reductase--genetics<br/>Folic Acid--blood<br/>Genetic Carrier Screening<br/>Genotype<br/>Heart Defects, Congenital--diagnosis<br/>Homocysteine--blood<br/>Homozygote<br/>Humans<br/>Infant<br/>Klinefelter Syndrome--diagnosis<br/>Male<br/>Meiosis<br/>Methylenetetrahydrofolate Reductase (NADPH2)--genetics<br/>Methylmalonic Acid--blood<br/>Nondisjunction, Genetic--genetics<br/>Polymorphism, Genetic--genetics<br/>Pregnancy<br/>Pregnancy in Adolescence--genetics<br/>Sex Chromosome Aberrations<br/>Trisomy