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Research 301–330 of 1000+
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Genetic mechanism of androgenic alopecia
- Recurrent Pregnancy Loss Associated Cytogenetic and Genetic Anomalies – Study from Eastern India
- Index of Suspicion
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- The Sex-Linked Histocompatibility Antigens
- Down Syndrome and Autoimmune Disease
- Genotoxicity of Rice Bran Oil Extracted by Supercritical CO<sub>2</sub> Extraction
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Ponatinib-induced pityriasis rubra pilaris-like adnexal dysmaturation: A case report
- Serum Androgens and Genetic Linkage Analysis in Early Onset Androgenetic Alopecia
- XX/XY chimerism in tortoiseshell tomcats – a new case and review of the literature
- Adult Patients with Aphallia: Were they Fertile?
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Eruptive syringomas in Down’s syndrome
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- PERBANDINGAN ARMS-PCR DAN ALLELE-SPECIFIC PCR DALAM OPTIMASI GENOTIPING SNP rs1998076
- Improving human forensics through advances in genetics, genomics and molecular biology
- Molecular basis of androgen insensitivity
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Gene Expression of Mouse S100A3, a Cysteine-Rich Calcium-Binding Protein, in Developing Hair Follicle