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Research 91–120 of 1000+
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- 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
- 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
- The Roles of EDA2R in Ageing and Disease
- Unusual Presentation of Childhood Leukemia With Vaginal Bleeding: A Case Report
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- 7 Pathogenesis and Classification of Male Pattern Hair Loss (Androgenic Alopecia)
- Cosmeceutical Treatments for Androgenetic Alopecia
- Secondary Cicatricial and other Permanent Alopecias
- 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
- DYS459, DYS391, DYS388 and DYS19 genetic loci have high allelic frequency in patients with prostate cancer
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Recurrent Pregnancy Loss Associated Cytogenetic and Genetic Anomalies – Study from Eastern India
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Adult Patients with Aphallia: Were they Fertile?
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Basonuclin is associated with the ribosomal RNA genes on human keratinocyte mitotic chromosomes
- 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
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Clinical Case Notes. Tamoxifen optic neuropathy
- Down Syndrome and Autoimmune Disease
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?