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pro vyhledávání: '"Shela Mohammed"'
Autor:
Ghazala Mirza, Jiannis Ragoussis, Ruth R Williams, Shari Baldinger, Frances Flinter, Robin Clark, Ruth Newbury-Ecob, Shela Mohammed
Publikováno v:
European Journal of Human Genetics. 12:718-728
Clinical reports of cases with deletions in chromosome 6p are relatively rare. We present a detailed study by fluorescent in situ hybridisation (FISH) of six new cases with distinct but overlapping 6p deletions involving the 6p24-pter chromosomal seg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::686c8c710eb175da33c9b992604c1a8f
https://doi.org/10.1038/sj.ejhg.5201194
https://doi.org/10.1038/sj.ejhg.5201194
