Case report: Neonatal diabetes mellitus with congenital hypothyroidism as a result of biallelic heterozygous mutations in GLIS3 gene
Perdas, Ewelina, Gadzalska, Karolina, Hrytsiuk, Ihor, Borowiec, Maciej, Fendler, Wojciech, Młynarski, Wojciech
Published in Pediatric diabetes (01.09.2022)
Published in Pediatric diabetes (01.09.2022)
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Case report: Neonatal diabetes mellitus with congenital hypothyroidism as a result of biallelic heterozygous mutations in GLIS3gene
Perdas, Ewelina, Gadzalska, Karolina, Hrytsiuk, Ihor, Borowiec, Maciej, Fendler, Wojciech, Młynarski, Wojciech
Published in Pediatric diabetes (01.09.2022)
Published in Pediatric diabetes (01.09.2022)
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Comment on: Congenital dyserythropoietic anemia type IV with KLF1 E325K mutation: A new case with dysmorphic male genitalia. Report of a second case
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Published in Pediatric blood & cancer (27.08.2024)
Published in Pediatric blood & cancer (27.08.2024)
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Use of selected types of crime analysis in modern criminological science
Topchii, Vasyl, Topchii, Oksana, Zabarniy, Maksym, Karpenko, Nataliіa, Hrytsiuk, Ihor
Published in Linguistics and Culture Review (23.11.2021)
Published in Linguistics and Culture Review (23.11.2021)
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Case report: Neonatal diabetes mellitus with congenital hypothyroidism as a result of biallelic heterozygous mutations in GLIS3 gene
Perdas, Ewelina, Gadzalska, Karolina, Hrytsiuk, Ihor, Borowiec, Maciej, Fendler, Wojciech, Młynarski, Wojciech
Published in Pediatric diabetes (01.09.2022)
Published in Pediatric diabetes (01.09.2022)
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No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome
Abo-Dalo, Benjamin, Roes, Melanie, Canún, Sonia, Delatycki, Martin, Gillessen-Kaesbach, Gabriele, Hrytsiuk, Ihor, Jung, Christine, Kerr, Bronwyn, Mowat, David, Seemanova, Eva, Steiner, Carlos E, Stewart, Helen, Thierry, Patrick, van Buggenhout, Griet, White, Sue, Zenker, Martin, Kutsche, Kerstin
Published in Clinical dysmorphology (01.07.2008)
Published in Clinical dysmorphology (01.07.2008)
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