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Research 901–930 of 1000+
- Disorders of Sex Development
- The genetics of androgenetic alopecia
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Psoriasis y alopecia areata con traquioniquia concurrente en una paciente pediátrica con síndrome de Turner
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- Coexistence of psoriasis, and alopecia areata with trachyonychia in a pediatric patient with Turner Syndrome
- It’s X-Related: Biological Bases of Increased COVID-19 Morbidity and Mortality in Men
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- 7 Pathogenesis and Classification of Male Pattern Hair Loss (Androgenic Alopecia)
- Social selection favours offspring prone to the development of androgenetic alopecia.
- Cosmeceutical Treatments for Androgenetic Alopecia
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Allelic frequencies for the seventeen Y-STR loci observed in Iraqi male patients with prostate cancer
- BIPHENOTYPIC LEUKAEMIA
- DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer
- 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
- 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
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- 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
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?