Marta Smyk

Institute of Mother and Child

Poland

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Articles (8)

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Collaborators (12)

Aleksandra Landowska

Instytut Matki i Dziecka

POLAND

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Piotr Wegrzyn

Professor, Head of Department

Medical University of Warsaw

POLAND

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Maria Sasiadek

Prof.

POLAND

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Krzysztof Szczałuba

assistant professor

Medical University of Warsaw

POLAND

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Marzena Debska

POLAND

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Katarzyna Niepokój

Institute of Mother and Child

POLAND

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Karolina Rutkowska

Medical University of Warsaw

POLAND

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Magdalena Bartnik-Głaska

Institute of Mother and Child

POLAND

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Agnieszka Różdżyńska-Świątkowska

PhD; Head of Anthropology Laboratory

Children's Memorial Health Institute

POLAND

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Tadeusz Issat

Instytut Matki i Dziecka

POLAND

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Anna Kutkowska-Kaźmierczak

Instytut Matki i Dziecka

POLAND

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Mateusz Dawidziuk

Instytut Matki i Dziecka

POLAND

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Marta Smyk

Research Interests

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Articles (8)

Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies

Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss

Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the <i>ANKRD11</i> Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3

Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities

Movement disorders associated with chromosomal aberrations diagnosed in adult patients

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Diverse clinical outcome of Hunter syndrome in patients with chromosomal aberration encompassing entire and partial IDS deletions: what is important for early diagnosis and counseling?

Null variants in AGRN cause lethal fetal akinesia deformation sequence

Collaborators (12)

Aleksandra Landowska

Piotr Wegrzyn

Maria Sasiadek

Krzysztof Szczałuba

Marzena Debska

Katarzyna Niepokój

Karolina Rutkowska

Magdalena Bartnik-Głaska

Agnieszka Różdżyńska-Świątkowska

Tadeusz Issat

Anna Kutkowska-Kaźmierczak

Mateusz Dawidziuk

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