Beata A. Nowakowska

17a Kasprzaka St
Warsaw, MZ 01211, Poland

Last Updated: 09/26/2026

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Found 70 publications

Prenatal Ultrasound and Genetic Diagnosis of EFTUD2 Haploinsufficiency in Two Fetuses: A Case Series.

Prenatal Ultrasound and Genetic Diagnosis of EFTUD2 Haploinsufficiency in Two Fetuses: A Case Series.

Journal: The application of clinical genetics
Published: November 14, 2025

Cytogenomic and Clinicopathologic Comparison of MYC-Positive and MYC-Negative High-Grade B-Cell Lymphoma With 11q Aberration in the Context of Other Aggressive Lymphomas With MYC Rearrangement.

Cytogenomic and Clinicopathologic Comparison of MYC-Positive and MYC-Negative High-Grade B-Cell Lymphoma With 11q Aberration in the Context of Other Aggressive Lymphomas With MYC Rearrangement.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: September 05, 2024

Valproic Acid Confers Functional Pluripotency to Human Amniotic Fluid Stem Cells in a Transgene-free Approach.

Valproic Acid Confers Functional Pluripotency to Human Amniotic Fluid Stem Cells in a Transgene-free Approach.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: August 09, 2024

Risk of meningomyelocele mediated by the common 22q11.2 deletion.

Risk of meningomyelocele mediated by the common 22q11.2 deletion.

Journal: Science (New York, N.Y.)
Published: May 02, 2024

COVID-19-related premature ovarian insufficiency: case report and literature review.

COVID-19-related premature ovarian insufficiency: case report and literature review.

Journal: Climacteric : the journal of the International Menopause Society
Published: August 30, 2023

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.

Journal: American journal of obstetrics and gynecology
Published: June 15, 2023

Identification and characterization of stromal-like cells with CD207+/low CD1a+/low phenotype derived from histiocytic lesions - a perspective in vitro model for drug testing.

Identification and characterization of stromal-like cells with CD207+/low CD1a+/low phenotype derived from histiocytic lesions - a perspective in vitro model for drug testing.

Journal: BMC cancer
Published: May 08, 2023

Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.

Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.

Journal: Genes
Published: November 21, 2022

Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.

Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome.

Journal: Genes
Published: November 19, 2022

Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.

Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 03, 2022

Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.

Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: May 03, 2022

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Journal: Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
Published: May 01, 2022
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Last Updated: 09/26/2026