LUIS
PAISAN GRISOLIA
Investigador/a en el periodo 1993-2009
C.
Nieto Conde
Publicaciones en las que colabora con C. Nieto Conde (4)
2008
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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, Vol. 146, Núm. 1, pp. 15-25
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Epidemiological association between isolated skin marks in newborn infants and single umbilical artery (SUA). Does it have biological plausibility?
American Journal of Medical Genetics, Part A, Vol. 146, Núm. 1, pp. 26-34
2006
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Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR geness: 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, Vol. 140 A, Núm. 9, pp. 987-997
1999
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Síndrome de Apert: análisis clínico-epidemiológico de una serie consecutiva de casos en España
Anales españoles de pediatría: Publicación oficial de la Asociación Española de Pediatría ( AEP ), Vol. 51, Núm. 6, pp. 667-683