Mihaela I. Gramescu

16 University Street
Iasi, IS 700115, Romania

Last Updated: 09/26/2026

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Found 11 publications

Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype-Phenotype Correlations, and Precision Medicine.

Molecular and Genetic Determinants of Nephrocalcinosis: Mechanisms, Genotype-Phenotype Correlations, and Precision Medicine.

Journal: International journal of molecular sciences

Published: March 21, 2026

Hydatidiform Mole-Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative Review.

Hydatidiform Mole-Between Chromosomal Abnormality, Uniparental Disomy and Monogenic Variants: A Narrative Review.

Journal: Life (Basel, Switzerland)

Published: September 28, 2023

A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.

A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.

Journal: Genes

Published: November 04, 2021

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review.

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review.

Journal: Children (Basel, Switzerland)

Published: July 01, 2021

Pallister-Killian Syndrome versus Trisomy 12p-A Clinical Study of 5 New Cases and a Literature Review.

Pallister-Killian Syndrome versus Trisomy 12p-A Clinical Study of 5 New Cases and a Literature Review.

Journal: Genes

Published: April 26, 2021

Dicentric Chromosome 14;18 Plus Two Additional CNVs in a Girl with Microform Holoprosencephaly and Turner Stigmata.

Dicentric Chromosome 14;18 Plus Two Additional CNVs in a Girl with Microform Holoprosencephaly and Turner Stigmata.

Journal: Balkan journal of medical genetics : BJMG

Published: April 30, 2014

Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.

Inverted duplication deletion of 8P: characterization by standard cytogenetic and SNP array analyses.

Journal: Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi

Published: February 08, 2014

Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature.

Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literature.

Journal: Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi

Published: February 08, 2014

Phenotypic variability in Patau syndrome.

Phenotypic variability in Patau syndrome.

Journal: Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi

Published: December 18, 2013

Ring autosomes: some unexpected findings.

Ring autosomes: some unexpected findings.

Journal: Balkan journal of medical genetics : BJMG

Published: September 21, 2013

Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome

Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome

Journal: Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi

Published: November 04, 2011

Showing 1-11 of 11

Last Updated: 09/26/2026