Kim Valérie van Berkel

Vrije Universiteit Brussel

Belgium

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Articles (9)

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2023

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2022

Year:

2022

Year:

2021

Year:

2021

Collaborators (17)

Kathelijn Keymolen

Vrije Universiteit Brussel

BELGIUM

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Nathalie Eduarda Marie-Jeanne Vanden Eynde

Vrije Universiteit Brussel

BELGIUM

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Nathalie Fieremans

Vrije Universiteit Brussel

BELGIUM

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Laure Dombrecht

Vrije Universiteit Brussel

BELGIUM

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Thomy de Ravel

Vrije Universiteit Brussel

BELGIUM

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Katrien Stouffs

Vrije Universiteit Brussel

BELGIUM

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Boyan Ivanov Dimitrov

Vrije Universiteit Brussel

BELGIUM

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Maaike Fobelets

Vrije Universiteit Brussel

BELGIUM

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Natália Oliva Teles

PORTUGAL

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An Vercoutere

Université libre de Bruxelles

BELGIUM

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Ann Van Den Bogaert

Vrije Universiteit Brussel

BELGIUM

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Ramses Forsyth

Vrije Universiteit Brussel

BELGIUM

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Leonardo GUCCIARDO

Vrije Universiteit Brussel

BELGIUM

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Sonia Van Dooren

Vrije Universiteit Brussel

BELGIUM

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Bettina Blaumeiser

University of Antwerp

BELGIUM

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Elisa Done

Vrije Universiteit Brussel

BELGIUM

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Ileen Slegers

Vrije Universiteit Brussel

BELGIUM

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Kim Valérie van Berkel

Research Interests

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Articles (9)

Searching for a sense of closure parental experiences of recontacting after a terminated pregnancy for congenital malformations

Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus

Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles

Pregnancy termination at a viable stage in daily clinical practice: A nationwide mortality follow‐back study in Flanders, Belgium

Identification of 16p11.2 microdeletions and microduplications in a cohort of individuals: a 2014-2021 retrospective analysis

Implementation of fetal clinical exome sequencing

Haemophagocytic lymphohistiocytosis during pregnancy: a case presentation and literature review

Novel Variant in COL4A1 Causes Extensive Prenatal Intracranial Hemorrhage and Porencephaly

A prenatal case of lissencephaly with cerebellar hypoplasia: New mutation in RELN gene

Collaborators (17)

Kathelijn Keymolen

Nathalie Eduarda Marie-Jeanne Vanden Eynde

Nathalie Fieremans

Laure Dombrecht

Thomy de Ravel

Katrien Stouffs

Boyan Ivanov Dimitrov

Maaike Fobelets

Natália Oliva Teles

An Vercoutere

Ann Van Den Bogaert

Ramses Forsyth

Leonardo GUCCIARDO

Sonia Van Dooren

Bettina Blaumeiser

Elisa Done

Ileen Slegers

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