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Research 181–210 of 1000+
- Fibrosing Frontal Alopecia: A comprehensive study to understand its etiology
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- Androgenetska alopecija u žena
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Genetics of Diabetes in Childhood
- Hair Today
- An Overview of Alopecias
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Developmental genetics of color pattern establishment in cats
- Tabby pattern genetics – a whole new breed of cat
- Past, Present and Future Perspectives of Forensic Genetics
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Analogs of human genetic skin disease in domesticated animals
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Ichthyosis with confetti: clinics, molecular genetics and management
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity