Identification of a Mosaic Variant in the SYNCRIP Gene Causing Foetal Periventricular Nodular Heterotopia, Abnormal Sulcation and Infratentorial Anomaly

Roee Birnbaum; Gustavo Malinger; Liat Ben Sira; Mirela Goldenberg-Furmanov; Hadas Miremberg; Mordechai Shohat; Karina Krajden Haratz

doi:10.1002/pd.6698

Identification of a Mosaic Variant in the SYNCRIP Gene Causing Foetal Periventricular Nodular Heterotopia, Abnormal Sulcation and Infratentorial Anomaly

Roee Birnbaum, Gustavo Malinger^*, Liat Ben Sira, Mirela Goldenberg-Furmanov, Hadas Miremberg, Mordechai Shohat, Karina Krajden Haratz

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1659-1662
Number of pages	4
Journal	Prenatal Diagnosis
Volume	44
Issue number	13
DOIs	https://doi.org/10.1002/pd.6698
State	Published - Dec 2024

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10.1002/pd.6698

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title = "Identification of a Mosaic Variant in the SYNCRIP Gene Causing Foetal Periventricular Nodular Heterotopia, Abnormal Sulcation and Infratentorial Anomaly",

author = "Roee Birnbaum and Gustavo Malinger and {Ben Sira}, Liat and Mirela Goldenberg-Furmanov and Hadas Miremberg and Mordechai Shohat and Haratz, {Karina Krajden}",

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AU - Ben Sira, Liat

AU - Goldenberg-Furmanov, Mirela

AU - Miremberg, Hadas

AU - Shohat, Mordechai

AU - Haratz, Karina Krajden

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Identification of a Mosaic Variant in the SYNCRIP Gene Causing Foetal Periventricular Nodular Heterotopia, Abnormal Sulcation and Infratentorial Anomaly

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