Zobrazeno 1 - 5
of 5
pro vyhledávání: '"P F R, Hochstenbach"'
Autor:
P F R Hochstenbach, Jacob A. S. Vorstman, W G Staal, H. van Engeland, Lude Franke, E van Daalen
Publikováno v:
Molecular Psychiatry. 11(1):18-28
The identification of the candidate genes for autism through linkage and association studies has proven to be a difficult enterprise. An alternative approach is the analysis of cytogenetic abnormalities associated with autism. We present a review of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19757cab53011a89462058c844de511d
https://doi.org/10.1038/sj.mp.4001757
https://doi.org/10.1038/sj.mp.4001757
Autor:
M T M, Franssen, J C, Korevaar, N J, Leschot, P M M, Bossuyt, A C, Knegt, K B J, Gerssen-Schoorl, C H, Wouters, K B M, Hansson, P F R, Hochstenbach, K, Madan, F, van der Veen, M, Goddijn
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 151(15)
To identify additional risk factors and the corresponding probability of carrying a chromosome abnormality in couples with two or more miscarriages.Nested case-control study.In 6 centres for clinical genetics in the Netherlands, data were collected f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::828c8b0a48e7ebc91cc3f85aa25ea323
https://pubmed.ncbi.nlm.nih.gov/18064941
https://pubmed.ncbi.nlm.nih.gov/18064941
Publikováno v:
Molecular psychiatry. 11(1)
The identification of the candidate genes for autism through linkage and association studies has proven to be a difficult enterprise. An alternative approach is the analysis of cytogenetic abnormalities associated with autism. We present a review of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ba3e943fbe00fa13c47091358bfadb20
https://pubmed.ncbi.nlm.nih.gov/16205736
https://pubmed.ncbi.nlm.nih.gov/16205736
Publikováno v:
Molecular Psychiatry. 11:1-1
Overview of cytogenetic regions of interest (CROIs) associated with the autism phenotype across the human genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4aedbe65af818ce3ccdefd5352382ffe
https://doi.org/10.1038/sj.mp.4001781
https://doi.org/10.1038/sj.mp.4001781
Publikováno v:
Histochemistry. 84:383-386
An X chromosome specific nucleic acid probe was used to study the positions of the X chromosomes in leukocyte nuclei by in situ hybridization to smears of peripheral blood. This autoradiographic approach allowed the first direct demonstration of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f053338c75707cde39bf3068a0df8ba
https://doi.org/10.1007/bf00482967
https://doi.org/10.1007/bf00482967