Items where the Publication is American journal of medical genetics Part A

Number of items: 5.
2009
  • Evaluation of folate metabolism gene polymorphisms as risk factors for open and closed neural tube defects. (2009) Doudney, K; Grinham, J; Whittaker, J; Lynch, SA; Thompson, D; Moore, GE; Copp, AJ; Greene, NDE; Stanier, P
  • Neuropsychological attention deficits in tuberous sclerosis complex (TSC). (2009) de Vries, Petrus J; Gardiner, Julian; Bolton, Patrick F
    • 2008
  • Does single umbilical artery (SUA) predict any type of congenital defect? Clinical-epidemiological analysis of a large consecutive series of malformed infants. (2008) Martínez-Frías, María Luisa; Bermejo, Eva; Rodríguez-Pinilla, Elvira; Prieto, David; ECEMC Working Group
    • 2006
  • Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome? (2006) Martínez-Frías, María-Luisa; Pérez, Belén; Desviat, Lourdes R; Castro, Margarita; Leal, Fátima; Rodríguez, Laura; Mansilla, Elena; Martínez-Fernández, María-Luisa; Bermejo, Eva; Rodríguez-Pinilla, Elvira; Prieto, David; Ugarte, Magdalena; ECEMC Working Group
  • Consanguineous marriage and congenital heart defects: a case-control study in the neonatal period. (2006) Yunis, Khalid; Mumtaz, Ghina; Bitar, Fadi; Chamseddine, Fadi; Kassar, May; Rashkidi, Joseph; Makhoul, Ghaith; Tamim, Hala