De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening

Chidinma Nwakalor; Sara Said-Delgado; Shifra Krinshpun; Milen Velinov

doi:10.1002/pd.5798

De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening

Chidinma Nwakalor, Sara Said-Delgado, Shifra Krinshpun, Milen Velinov

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

Original language	English (US)
Pages (from-to)	11-14
Number of pages	4
Journal	Prenatal Diagnosis
Volume	41
Issue number	1
DOIs	https://doi.org/10.1002/pd.5798
State	Published - Jan 2021
Externally published	Yes

All Science Journal Classification (ASJC) codes

Obstetrics and Gynecology
Genetics(clinical)

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10.1002/pd.5798

Cite this

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title = "De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening",

author = "Chidinma Nwakalor and Sara Said-Delgado and Shifra Krinshpun and Milen Velinov",

year = "2021",

month = jan,

doi = "10.1002/pd.5798",

language = "English (US)",

volume = "41",

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journal = "Prenatal Diagnosis",

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publisher = "John Wiley and Sons Ltd",

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AU - Nwakalor, Chidinma

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AU - Krinshpun, Shifra

AU - Velinov, Milen

PY - 2021/1

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SN - 0197-3851

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SP - 11

EP - 14

JO - Prenatal Diagnosis

JF - Prenatal Diagnosis

IS - 1

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De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening

All Science Journal Classification (ASJC) codes

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