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Phenotypic spectrum of NDE1‐related disorders: from microlissencephaly to microhydranencephaly |
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| Authors: | Mohamed S. Abdel‐Hamid Sara H. El‐Dessouky Mohamed I. Ateya Hassan M. Gaafar Ghada M.H. Abdel‐Salam |
| Affiliation: | 1. https://orcid.org/0000-0002-2480-0147;2. Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt;3. Ghada M.H. Abdel‐Salam, Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Tahrir street, Dokki, Cairo, Egypt.;4. and;5. Mohamed S. Abdel‐Hamid, Medical Molecular Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Tahrir street, Dokki, Cairo, Egypt.;6. Prenatal Diagnosis and Fetal Medicine Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt;7. Fetal Medicine Unit, Cairo University, Cairo, Egypt;8. https://orcid.org/0000-0003-2893-8802;9. Clinical Genetics Department, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt |
| Abstract: | |
| Keywords: | fusion of thalami microcephaly microhydranencephaly microlissencephaly NDE1 prenatal ultrasound |