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Research 211–240 of 1000+
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- 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
- British Society for Dermatopathology
- Molecular genetics of androgen insensitivity
- 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
- Disorders of Sex Development
- Secondary Cicatricial and other Permanent Alopecias
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- ROBERTSONIAN TRANSLOCATION PATIENT WITH RECURRENT MISCARRIAGE
- Allelic frequencies for the seventeen Y-STR loci observed in Iraqi male patients with prostate cancer
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- BIPHENOTYPIC LEUKAEMIA
- DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer
- 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
- 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
- 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