Found: 12
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Intellectual Disability and Blended Phenotypes: Insights from a Centre in North India.
- Published in:
- Case Reports in Genetics, 2024, v. 2024, p. 1, doi. 10.1155/2024/6009569
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- Article
A De Novo Missense MYLK Variant Leading to Nonsyndromic Thoracic Aortic Aneurysm and Dissection Identified by Segregation Analysis.
- Published in:
- Case Reports in Genetics, 2024, v. 2024, p. 1, doi. 10.1155/2024/4281972
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- Article
Two Pediatric Cases of Primary Ciliary Dyskinesia Caused by Loss‐of‐Function Variants in Oral‐Facial‐Digital Syndrome Gene, OFD1.
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- Case Reports in Genetics, 2024, v. 2024, p. 1, doi. 10.1155/2024/1595717
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- Article
Discovery of a Novel DYRK1A Mutation (c.524del) in Intellectual Development Disorder Autosomal Dominant 7 (MRD7): A Comprehensive Case Analysis.
- Published in:
- Case Reports in Genetics, 2024, v. 2024, p. 1, doi. 10.1155/2024/2926555
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- Article
Phenotype‐Genotype Discordance and a Case of a Disorder of Sexual Differentiation.
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- Case Reports in Genetics, 2024, v. 2024, p. 1, doi. 10.1155/2024/9936936
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- Article
A Fatal Case of 3‐Hydroxyisobutyryl‐CoA Hydrolase Deficiency in a Term Infant with Severe High Anion Gap Acidosis and Review of the Literature.
- Published in:
- Case Reports in Genetics, 2024, v. 2024, p. 1, doi. 10.1155/2024/8099373
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- Article
Quadruple Primary Malignancies over 2 Years with Germline Mutation in Krebs Cycle Enzyme Gene Fumarate Hydratase.
- Published in:
- Case Reports in Genetics, 2024, v. 2024, p. 1, doi. 10.1155/2024/5591237
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- Article
Mitochondrial DNA Missense Mutations ChrMT: 8981A > G and ChrMT: 6268C > T Identified in a Caucasian Female with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Triggered by the Epstein–Barr Virus.
- Published in:
- Case Reports in Genetics, 2024, v. 2024, p. 1, doi. 10.1155/2024/6475425
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- Article
Bilateral Glaucoma as Possible Additional Feature for PGAP3-Associated Hyperphosphatasia.
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- 2024
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- Publication type:
- Case Study
Genital Abnormalities and Growth Retardation as Early Signs of Dilated Cardiomyopathy with Ataxia Syndrome.
- Published in:
- 2024
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- Publication type:
- Case Study
A Novel Heterozygous De Novo MORC2 Missense Variant Causes an Early Onset and Severe Neurodevelopmental Disorder.
- Published in:
- 2024
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- Publication type:
- Case Study
Constitutional Chromothripsis on Chromosome 2: A Rare Case with Severe Presentation.
- Published in:
- 2024
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- Publication type:
- Case Study