kw.\*:("Origen materno")
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Non-genetic inheritable potential of maternal antibodiesLEMKE, Hilmar; HANSEN, Hinrich; LANGE, Hans et al.Vaccine. 2003, Vol 21, Num 24, pp 3428-3431, issn 0264-410X, 4 p.Conference Paper
Recurrent triploidy of maternal originBRANCATI, Francesco; MINGARELLI, Rita; DALLAPICCOLA, Bruno et al.European journal of human genetics. 2003, Vol 11, Num 12, pp 972-974, issn 1018-4813, 3 p.Article
A case of 49,XXXXX in which the extra X chromosomes were maternal in originCHO, Y. G; KIM, D. S; LEE, H. S et al.Journal of clinical pathology. 2004, Vol 57, Num 9, pp 1004-1006, issn 0021-9746, 3 p.Article
Lack of imprinting of the human dopamine D4 receptor (DRD4) geneCICHON, S; NÖTHEN, M. M; WOLF, H. K et al.American journal of medical genetics. 1996, Vol 67, Num 2, pp 229-231, issn 0148-7299Article
Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q)STALLARD, R; KRUEGER, S; JAMES, R. S et al.American journal of medical genetics. 1995, Vol 57, Num 1, pp 14-18, issn 0148-7299Article
Intragenomic conflict and the evolution of eusocialityHAIG, D.Journal of theoretical biology. 1992, Vol 156, Num 3, pp 401-403, issn 0022-5193Article
CDG-Id caused by homozygosity for an ALG3 mutation due to segmental maternal isodisomy UPD3(q21.3-qter)SCHOLLEN, E; GRÜNEWALD, S; KELDERMANS, L et al.European journal of medical genetics. 2005, Vol 48, Num 2, pp 153-158, issn 1769-7212, 6 p.Article
Immunité maternelle chez le nouveau-né de Poecilia reticulataTAKAHASHI, Y; KAWAHARA, E.Nippon Suisan Gakkaishi. 1987, Vol 53, Num 5, pp 721-725, issn 0021-5392Article
Widespread Monoallelic Expression on Human AutosomesGIMELBRANT, Alexander; HUTCHINSON, John N; THOMPSON, Benjamin R et al.Science (Washington, D.C.). 2007, Vol 318, Num 5853, pp 1136-1140, issn 0036-8075, 5 p.Article
Patterns of maternal transmission in bipolar affective disorderMCMAHON, F. J; STINE, O. C; MEYERS, D. A et al.American journal of human genetics. 1995, Vol 56, Num 6, pp 1277-1286, issn 0002-9297Article
The maternal-zygotic transition : Death and birth of RNAs : Germ cellsSCHIER, Alexander F.Science (Washington, D.C.). 2007, Vol 316, Num 5823, pp 406-407, issn 0036-8075, 2 p.Article
Mechanisms by which maternal antibodies influence infant vaccine responses: review of hypotheses and definition of main determinantsSIEGRIST, Claire-Anne.Vaccine. 2003, Vol 21, Num 24, pp 3406-3412, issn 0264-410X, 7 p.Conference Paper
A simple and effective approach for detecting maternal cell contamination in molecular prenatal diagnosisANTONIADI, T; YAPIJAKIS, C; KAMINOPETROS, P et al.Prenatal diagnosis. 2002, Vol 22, Num 5, pp 425-429, issn 0197-3851Article
Founding mothers of Jewish communities: Geographically separated Jewish groups were independently founded by very few female ancestorsTHOMAS, Mark G; WEALE, Michael E; WILSON, James F et al.American journal of human genetics. 2002, Vol 70, Num 6, pp 1411-1420, issn 0002-9297Article
The evolutionary origins of maternal calcium and bone metabolism during lactationWYSOLMERSKI, John J.Journal of mammary gland biology and neoplasia. 2002, Vol 7, Num 3, pp 267-276, issn 1083-3021, 10 p.Article
Higher risk of seizures in offspring of mothers than of fathers with epilepsyOTTMAN, R; ANNEGERS, J. F; HAUSER, W. A et al.American journal of human genetics. 1988, Vol 43, Num 3, pp 257-264, issn 0002-9297Article
Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size rangeSULLIVAN, Amy K; CRAWFORD, Dana C; SCOTT, Elizabeth H et al.American journal of human genetics. 2002, Vol 70, Num 6, pp 1532-1544, issn 0002-9297Article
Les thrombopénies périnatales d'origine maternelle = Maternal causes of perinatal thrombocytopeniaCHANTRAIN, C; DEBAUCHE, C; LANGHENDRIES, J. P et al.Archives de pédiatrie (Paris). 2000, Vol 7, Num 7, pp 756-762, issn 0929-693XArticle
Maternal origin of nucleated erythrocytes in peripheral venous blood of pregant womenSLUNGA-TALLBERG, A; EL-RIFAI, W.'E; KEINÄNEN, M et al.Human genetics. 1995, Vol 96, Num 1, pp 53-57, issn 0340-6717Article
Fetal hypokinesia sequence caused by maternal autoimmune disorder ?HENNEKAM, R. C. M; ROTTEVEEL, J. J; HALL, J. G et al.American journal of medical genetics. 1992, Vol 43, Num 6, pp 1047-1048, issn 0148-7299Article
Influence of diandric and digynic triploid genotypes on early mouse embryogenesisKAUFMAN, M. H; LEE, K. K. H; SPEIRS, S et al.Development (Cambridge). 1989, Vol 105, Num 1, pp 137-145Article
Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial TRNAHis geneXUKUN YAN; XINJIAN WANG; MINGZHI SUN et al.Journal of medical genetics. 2011, Vol 48, Num 10, pp 682-690, issn 0022-2593, 9 p.Article
Sex biases in the mutation rateHURST, K. D; ELLEGREN, H.Trends in genetics (Regular ed.). 1998, Vol 14, Num 11, pp 446-452, issn 0168-9525Article
Trisomy 18 : studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunctionFISHER, J. M; HARVEY, J. F; MORTON, N. E et al.American journal of human genetics. 1995, Vol 56, Num 3, pp 669-675, issn 0002-9297Article
Molecular studies of trisomy 18FISHER, J. M; HARVEY, J. F; LINDENBAUM, R. H et al.American journal of human genetics. 1993, Vol 52, Num 6, pp 1139-1144, issn 0002-9297Article