Browse by Publication
![]() | Up a level |
Number of items: 5.
D
Doudney, K;
Grinham, J;
Whittaker, J;
Lynch, SA;
Thompson, D;
Moore, GE;
Copp, AJ;
Greene, NDE;
Stanier, P;
(2009)
Evaluation of Folate Metabolism Gene Polymorphisms as Risk Factors for Open and Closed Neural Tube Defects.
American journal of medical genetics Part A, 149A (7).
pp. 1585-1589.
ISSN 1552-4825
DOI: https://doi.org/10.1002/ajmg.a.32937
Full text not available from this repository.
de Vries, PJ;
Gardiner, J;
Bolton, PF;
(2009)
Neuropsychological Attention Deficits in Tuberous Sclerosis Complex (TSC).
American journal of medical genetics Part A, 149A (3).
pp. 387-395.
ISSN 1552-4825
DOI: https://doi.org/10.1002/ajmg.a.32690
Full text not available from this repository.
M
Martínez-Frías, ML;
Bermejo, E;
Rodríguez-Pinilla, E;
Prieto, D;
ECEMC Working Group;
(2008)
Does single umbilical artery (SUA) predict any type of congenital defect? Clinical-epidemiological analysis of a large consecutive series of malformed infants.
American journal of medical genetics Part A, 146A (1).
pp. 15-25.
ISSN 1552-4825
DOI: https://doi.org/10.1002/ajmg.a.31911
Full text not available from this repository.
Martínez-Frías, ML;
Pérez, B;
Desviat, LR;
Castro, M;
Leal, F;
Rodríguez, L;
Mansilla, E;
Martínez-Fernández, ML;
Bermejo, E;
Rodríguez-Pinilla, E;
+3 more...
Prieto, D;
Ugarte, M;
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?
American journal of medical genetics Part A, 140 (9).
pp. 987-97.
ISSN 1552-4825
DOI: https://doi.org/10.1002/ajmg.a.31203
Full text not available from this repository.
Y
Yunis, K;
Khalid, Y;
Mumtaz, G;
Ghina, M;
Bitar, F;
Fadi, B;
Chamseddine, F;
Fadi, C;
Kassar, M;
May, K;
+6 more...
Rashkidi, J;
Joseph, R;
Makhoul, G;
Makhoul, G;
Tamim, H;
Hala, T;
(2006)
Consanguineous marriage and congenital heart defects: a case-control study in the neonatal period.
American journal of medical genetics Part A, 140 (14).
pp. 1524-30.
ISSN 1552-4825
DOI: https://doi.org/10.1002/ajmg.a.31309
Full text not available from this repository.