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Konservatif Yönetilen Ağır Preeklamptik Gebeliklerde Fetal Büyüme Kısıtlılığının Maternal ve Fetal Sonuçlar Üzerine Etkisi.
- Published in:
- Medical Journal of Istanbul Kanuni Sultan Süleyman / İstanbul Kanuni Sultan Süleyman Tıp Dergisi, 2022, v. 14, n. 1, p. 52, doi. 10.14744/iksstd.2021.91489
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- Publication type:
- Article
Evidence for correlations between BMI-associated SNPs and circRNAs.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-16495-7
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- Publication type:
- Article
Nadir Bir Olgu: Ilk Gebelikte Spontan Uterus Rüptürü.
- Published in:
- 2014
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- Publication type:
- Case Study
Sonographic features and management options of uterine arteriovenous malformation. A case report.
- Published in:
- 2015
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- Publication type:
- journal article
Prenatal diagnosis of congenital high airway obstruction syndrome (CHAOS). Five case report.
- Published in:
- Medical Ultrasonography, 2015, v. 17, n. 1, p. 115, doi. 10.11152/mu.2013.2066.171.haek
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- Publication type:
- Article
Comparison of fetal cardiac functions between small-for-gestational age fetuses and late-onset growth-restricted fetuses.
- Published in:
- Journal of Perinatal Medicine, 2019, v. 47, n. 8, p. 879, doi. 10.1515/jpm-2019-0206
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- Publication type:
- Article
Imprinting of RB1 (the new kid on the block).
- Published in:
- Briefings in Functional Genomics, 2010, v. 9, n. 4, p. 347, doi. 10.1093/bfgp/elq014
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- Publication type:
- Article
The Origin of the <i>RB1</i> Imprint.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0081502
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- Publication type:
- Article
Human <i>PPP1R26P1</i> Functions as <i>cis</i>-Repressive Element in Mouse <i>Rb1</i>.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0074159
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- Publication type:
- Article
RB1 -Negative Retinal Organoids Display Proliferation of Cone Photoreceptors and Loss of Retinal Differentiation.
- Published in:
- Cancers, 2022, v. 14, n. 9, p. N.PAG, doi. 10.3390/cancers14092166
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- Publication type:
- Article
Introduction of a Variant Classification System for Analysis of Genotype-Phenotype Relationships in Heritable Retinoblastoma.
- Published in:
- Cancers, 2021, v. 13, n. 7, p. 1605, doi. 10.3390/cancers13071605
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- Publication type:
- Article
Clinical utility gene card for: Angelman Syndrome.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 2, p. 1, doi. 10.1038/ejhg.2014.93
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- Publication type:
- Article
Novel deletions affecting the MEG3-DMR provide further evidence for a hierarchical regulation of imprinting in 14q32.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 2, p. 180, doi. 10.1038/ejhg.2014.72
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- Publication type:
- Article
Clinical utility gene card for: Prader-Willi Syndrome.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 9, p. -1, doi. 10.1038/ejhg.2014.66
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- Publication type:
- Article
Genotype-phenotype correlations in patients with retinoblastoma and interstitial 13q deletions.
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 9, p. 947, doi. 10.1038/ejhg.2011.58
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- Publication type:
- Article
A paternal deletion of MKRN3, MAGEL2 and NDN does not result in Prader–Willi syndrome.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 5, p. 582, doi. 10.1038/ejhg.2008.232
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- Publication type:
- Article
Low frequency of imprinting defects in ICSI children born small for gestational age.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 1, p. 22, doi. 10.1038/ejhg.2008.177
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- Publication type:
- Article
IGF2/H19 hypomethylation in Silver–Russell syndrome and isolated hemihypoplasia.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 3, p. 328, doi. 10.1038/sj.ejhg.5201974
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- Publication type:
- Article
13q deletion syndrome resulting from balanced chromosomal rearrangement in father: the significance of parental karyotyping.
- Published in:
- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00500-7
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- Publication type:
- Article
Fetal conotruncal heart anomalies: is four-chamber view sufficient in the prenatal screening?
- Published in:
- Perinatal Journal / Perinatoloji Dergisi, 2019, v. 27, n. 2, p. 113, doi. 10.2399/prn.19.0272010
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- Publication type:
- Article
Deciphering the evolutionary origin of the RB1 imprint.
- Published in:
- 2013
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- Publication type:
- Conference Paper/Materials
Author Correction: A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma.
- Published in:
- 2024
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- Publication type:
- Correction Notice
A MYCN-driven de-differentiation profile identifies a subgroup of aggressive retinoblastoma.
- Published in:
- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06596-6
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- Publication type:
- Article
Evolutionary Origin and Methylation Status of Human Intronic CpG Islands that Are Not Present in Mouse.
- Published in:
- Genome Biology & Evolution, 2014, v. 6, n. 7, p. 1579, doi. 10.1093/gbe/evu125
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- Publication type:
- Article
Is there a relationship between decreased humanin levels in gestational diabetes mellitus women requiring insulin treatment?
- Published in:
- Perinatal Journal, 2023, v. 31, n. 3, p. 207, doi. 10.59215/prn.23.0313005
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- Publication type:
- Article
The maternal uniparental disomy of chromosome 6 (upd(6)mat) 'phenotype': result of placental trisomy 6 mosaicism?
- Published in:
- Molecular Genetics & Genomic Medicine, 2017, v. 5, n. 6, p. 668, doi. 10.1002/mgg3.324
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- Publication type:
- Article
Clinical relevance of postzygotic mosaicism in Cornelia de Lange syndrome and purifying selection of NIPBL variants in blood.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-94958-z
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- Publication type:
- Article
Does maternal hyperoxygenation have any effect on the fetal circulatory system in normal growth and late-onset IUGR fetuses?
- Published in:
- Annals of Medical of Research, 2023, v. 30, n. 10, p. 1295, doi. 10.5455/annalsmedres.2023.08.228
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- Publication type:
- Article
Prenatal diagnosis of left pulmonary artery sling and review of literature.
- Published in:
- Echocardiography, 2019, v. 36, n. 5, p. 1001, doi. 10.1111/echo.14325
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- Publication type:
- Article
The Human Retinoblastoma Gene Is Imprinted.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 12, p. 1, doi. 10.1371/journal.pgen.1000790
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- Publication type:
- Article
Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprinted DLK1/GTL2 gene cluster.
- Published in:
- Human Mutation, 2008, v. 29, n. 9, p. 1141, doi. 10.1002/humu.20771
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- Publication type:
- Article
A novel large deletion of the ICR1 region including H19 and putative enhancer elements.
- Published in:
- BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0173-2
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- Publication type:
- Article