Deciphering copy number variations and gene implications in an Egyptian cohort with autism spectrum disorders.
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| Title: | Deciphering copy number variations and gene implications in an Egyptian cohort with autism spectrum disorders. |
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| Authors: | Mohamed AM; Human Cytogenetic Department, National Research Centre, Cairo, Egypt. amalmahmoud15@yahoo.com., Eid OM; Human Cytogenetic Department, National Research Centre, Cairo, Egypt., Amr KS; Department of Molecular and Medical Genetics, National Research Centre, Cairo, Egypt., Mahrous R; Human Cytogenetic Department, National Research Centre, Cairo, Egypt., Hemimi M; Research on Children with Special Needs Department, National Research Centre, Cairo, Egypt., Elsaeid A; Research on Children with Special Needs Department, National Research Centre, Cairo, Egypt., Erian PSF; Human Cytogenetic Department, National Research Centre, Cairo, Egypt., Gharib S; Human Cytogenetic Department, National Research Centre, Cairo, Egypt., Hussein SH; Human Cytogenetic Department, National Research Centre, Cairo, Egypt., El-Massieh PMA; Oro-dental Genetics Department, National Research Centre, Cairo, Egypt., Meguid NA; Research on Children with Special Needs Department, National Research Centre, Cairo, Egypt. |
| Source: | BMC medical genomics [BMC Med Genomics] 2025 Nov 27; Vol. 18 (1), pp. 190. Date of Electronic Publication: 2025 Nov 27. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794 (Electronic) Linking ISSN: 17558794 NLM ISO Abbreviation: BMC Med Genomics Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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