Chromosome 22 microdeletion in children with syndromic congenital heart disease by fluorescent in situ hybridization (FISH)

Soheir S.A. El-Ella; Fady El Gendy; Maha A.M. Tawfik; Ezzat El Sobky; Ahmed Khattab; Mohamed El-mekkawy

doi:10.1016/j.ejmhg.2012.04.006

Q2 2012

Chromosome 22 microdeletion in children with syndromic congenital heart disease by fluorescent in situ hybridization (FISH)

Soheir S.A. El-Ella · Fady El Gendy · Maha A.M. Tawfik · Ezzat El Sobky · Ahmed Khattab · Mohamed El-mekkawy

10.1016/j.ejmhg.2012.04.006 388 المشاهدات 1 الاقتباسات

الاقتباسات

388

المشاهدات

الملخص غير متوفر لهذا المنشور.

الاستشهاد بهذا المقال (APA)

Soheir, S. E., Fady, E. G., Maha, A. T., Ezzat, E. S., Ahmed, K., Mohamed, E. (2012). Chromosome 22 microdeletion in children with syndromic congenital heart disease by fluorescent in situ hybridization (FISH). Egyptian Journal of Medical Human Genetics. https://doi.org/10.1016/j.ejmhg.2012.04.006

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Reduced penetrance in human inherited disease