14 Artikel
Original Article
Uneingeschränkter Zugang | 05. Juni 2022
Clinical Experience of Neurological Mitochondrial Diseases in Children and Adults: A Single-Center Study
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Uneingeschränkter Zugang | 05. Juni 2022
Array-Based Comparative Genomic Hybridization Analysis in Children with Developmental Delay/Intellectual Disability
, , , , , und
Uneingeschränkter Zugang | 05. Juni 2022
Determination of Cystic Fibrosis Mutation Frequency in Preterm and Term Neonates with Respiratory Tract Problems
, und
Uneingeschränkter Zugang | 05. Juni 2022
Single-Nucleotide Polymorphisms in Exonic and Promoter Regions of Transcription Factors of Second Heart Field Associated with Sporadic Congenital Cardiac Anomalies
, , , und
Uneingeschränkter Zugang | 05. Juni 2022
Risk Factors of Venous Thromboembolism in Sudanese Pregnant Women
, , , , , , und
Uneingeschränkter Zugang | 05. Juni 2022
Targeted microRNA Profiling in Gastric Cancer with Clinical Assessement
, , , , , und
Uneingeschränkter Zugang | 05. Juni 2022
Association of Relative Telomere Length and Risk of High Human Papillomavirus Load in Cervical Epithelial Cells
und
Case Report
Uneingeschränkter Zugang | 05. Juni 2022
Phenotypic Variability of 17q12 Microdeletion Syndrome – Three Cases and Review of Literature
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Uneingeschränkter Zugang | 05. Juni 2022
Having Multiple Renal Cysts in a Young Adult is Not Always a Sign of Polycystic Kidney Disease
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Uneingeschränkter Zugang | 05. Juni 2022
de novo TINF2 C.845G>A: Pathogenic Variant in Patient with Dyskeratosis Congenita
, , , , und
Uneingeschränkter Zugang | 05. Juni 2022
Novel GPC3 Gene Mutation in Simpson-Golabi-Behmel Syndrome with Endocrine Anomalies: A Case Report
, , , und
Uneingeschränkter Zugang | 05. Juni 2022
Case Report for Two Siblings Carrying Neurofibromatosis Type 1 with a Rare NF1 : c.5392C>T Mutation
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