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A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.

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Title: A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.
Authors: Arefzadeh, Maryam1 (AUTHOR), Rabbani, Bahareh2 (AUTHOR), Abdolahpour, Saeideh2 (AUTHOR), Emami, Farnoosh2 (AUTHOR), Abbasi, Farzaneh2 (AUTHOR), Masoumi, Tannaz1 (AUTHOR), Mirab Samiee, Siamak3 (AUTHOR), Rabbani, Ali2 (AUTHOR), Mahdieh, Nejat3 (AUTHOR) nmahdieh@yahoo.com
Source: Clinical Case Reports. Mar2026, Vol. 14 Issue 3, p1-5. 5p.
Database: Academic Search Ultimate
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  Data: A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.
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  Data: <searchLink fieldCode="AR" term="%22Arefzadeh%2C+Maryam%22">Arefzadeh, Maryam</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rabbani%2C+Bahareh%22">Rabbani, Bahareh</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Abdolahpour%2C+Saeideh%22">Abdolahpour, Saeideh</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Emami%2C+Farnoosh%22">Emami, Farnoosh</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Abbasi%2C+Farzaneh%22">Abbasi, Farzaneh</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Masoumi%2C+Tannaz%22">Masoumi, Tannaz</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mirab+Samiee%2C+Siamak%22">Mirab Samiee, Siamak</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Rabbani%2C+Ali%22">Rabbani, Ali</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mahdieh%2C+Nejat%22">Mahdieh, Nejat</searchLink><relatesTo>3</relatesTo> (AUTHOR)<i> nmahdieh@yahoo.com</i>
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  Data: <searchLink fieldCode="JN" term="%22Clinical+Case+Reports%22">Clinical Case Reports</searchLink>. Mar2026, Vol. 14 Issue 3, p1-5. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=192557494
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        Value: 10.1002/ccr3.72218
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        Text: English
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      – TitleFull: A Novel Homozygous CUL7 Variant in an Iranian Patient Expands the Genetic Spectrum of 3 M Syndrome.
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              Text: Mar2026
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              Y: 2026
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