Found: 13
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Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome.
- Published in:
- Case Reports in Obstetrics & Gynecology, 2019, p. 1, doi. 10.1155/2019/6753184
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- Publication type:
- Article
Expression of proliferation markers in human pituitary incidentalomas.
- Published in:
- Endocrine Pathology, 2006, v. 17, n. 3, p. 263, doi. 10.1385/EP:17:3:263
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- Publication type:
- Article
Immunonegative null cell″adenomas and Gnadotropin (G) Subunit (Su) immunopositive adenomas share frequent expression of multiple transcription factors.
- Published in:
- Endocrine Pathology, 2006, v. 17, n. 1, p. 35, doi. 10.1385/EP:17:1:35
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- Publication type:
- Article
Uterine leiomyoma confounding a noninvasive prenatal test result.
- Published in:
- 2015
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- Publication type:
- case study
Induction of GH, PRL, and TSHβ mRNA by transfection of Pit-1 in a human pituitary adenoma-derived cell line.
- Published in:
- Cell & Tissue Research, 2005, v. 322, n. 2, p. 269, doi. 10.1007/s00441-005-0033-z
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- Publication type:
- Article
Novel large deletion involving EVC and EVC2 in Ellis–van Creveld syndrome.
- Published in:
- Human Genome Variation, 2022, v. 9, n. 1, p. 1, doi. 10.1038/s41439-022-00190-0
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- Publication type:
- Article
Genotype-phenotype correlation of renal lesions in the tuberous sclerosis complex.
- Published in:
- Human Genome Variation, 2022, v. 9, n. 1, p. 1, doi. 10.1038/s41439-022-00181-1
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- Publication type:
- Article
Dietary Soybean Enhances Pit-1 Dependent Pituitary Hormone Production in Iodine Deficient Rats.
- Published in:
- Journal of Molecular Histology, 2005, v. 36, n. 4, p. 265, doi. 10.1007/s10735-005-4710-8
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- Publication type:
- Article
Usefulness of combined NGS and QF‐PCR analysis for product of conception karyotyping.
- Published in:
- Reproductive Medicine & Biology, 2022, v. 21, n. 1, p. 1, doi. 10.1002/rmb2.12449
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- Publication type:
- Article
Transport and Golgi organization 2 deficiency with a prominent elevation of C14:1 during a metabolic crisis: A case report.
- Published in:
- 2023
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- Publication type:
- Case Study
Novel compound heterozygous mutations in the PLEC gene in a neonate with epidermolysis bullosa simplex with pyloric atresia.
- Published in:
- Journal of Dermatology, 2023, v. 50, n. 2, p. 239, doi. 10.1111/1346-8138.16553
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- Publication type:
- Article
Incontinentia pigmenti in a female infant with somatic mosaicism due to the IKBKG variant.
- Published in:
- Journal of Dermatology, 2021, v. 48, n. 12, p. e577, doi. 10.1111/1346-8138.16141
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- Publication type:
- Article
Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases.
- Published in:
- Cytogenetic & Genome Research, 2020, v. 160, n. 3, p. 118, doi. 10.1159/000507177
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- Publication type:
- Article