Found: 22
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Cover.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2137
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- Publication type:
- Article
MiR‐497‐5p inhibits cell proliferation and metastasis in hepatocellular carcinoma by targeting insulin‐like growth factor 1.
- Published in:
- 2023
- Publication type:
- Correction Notice
The compound heterozygous mutations of c.607G>a and c.657delC in the FAH gene are associated with renal damage with hereditary tyrosinemia type 1 (HT1).
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2090
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- Publication type:
- Article
Long non‐coding RNA NORAD promotes the occurrence and development of non‐small cell lung cancer by adsorbing MiR‐656‐3p.
- Published in:
- 2023
- Publication type:
- Correction Notice
MiR‐191‐5p inhibits lung adenocarcinoma by repressing SATB1 to inhibit Wnt pathway.
- Published in:
- 2023
- Publication type:
- Correction Notice
Association of demographic and clinical factors with risk of acute pancreatitis: An exposure‐wide Mendelian randomization study.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2091
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- Publication type:
- Article
BEST1 novel mutation causes Bestrophinopathies in six families with distinct phenotypic diversity.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2095
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- Publication type:
- Article
LncRNA SNHG4 promotes osteosarcoma proliferation and migration by sponging miR‐377‐3p.
- Published in:
- 2023
- Publication type:
- Correction Notice
Frataxin deficiency alters gene expression in Friedreich ataxia derived IPSC‐neurons and cardiomyocytes.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2093
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- Publication type:
- Article
Compound heterozygous loss‐of‐function variants in BRAT1 cause lethal neonatal rigidity and multifocal seizure syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2092
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- Publication type:
- Article
Using reported pathogenic variants to identify therapeutic opportunities for genetic diseases.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2097
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- Publication type:
- Article
Single nucleotide polymorphisms of PCP pathway related genes participate in the occurrence and development of neural tube defect.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2094
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- Publication type:
- Article
Estimate of genetic variants using CNV‐Seq for fetuses with oligohydramnios or polyhydramnios.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2089
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- Publication type:
- Article
Identification of Biallelic dystrophin gene variants during maternal carrier testing for Becker muscular dystrophy and review of the DMD exon 49–51 deletion phenotype.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2088
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- Publication type:
- Article
Same family, same mutation, different ECG.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2079
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- Publication type:
- Article
Characterization of health concerns in people with neurofibromatosis type 1.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2077
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- Publication type:
- Article
Management of methylmalonic acidemia (MMA) with N‐carbamylglutamate: A case report from Italy.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2073
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- Publication type:
- Article
The effect of growth hormone treatment in children with novel BPTF gene variants: A report of two cases and literature review.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2066
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- Publication type:
- Article
A novel SYNJ1 homozygous variant causing developmental and epileptic encephalopathy in an Afro‐Caribbean individual.
- Published in:
- 2023
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- Publication type:
- Case Study
Kearns‐Sayre syndrome case. Novel 5,9 kb mtDNA deletion.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2059
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- Publication type:
- Article
Not just a carrier: Clinical presentation and management of patients with heterozygous disease‐causing alkaline phosphatase (ALPL) variants identified through expanded carrier screening.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.2056
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- Publication type:
- Article
Issue Information.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 1, p. 1, doi. 10.1002/mgg3.1973
- Publication type:
- Article