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Research 31–60 of 1000+
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Phenotypic, transcriptomic, and genomic analyses reveal the spatiotemporal patterns and associated genes of coarse hair density in goats
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- The hair shaft: normality, abnormality, and genetics
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Gene Expression of Mouse S100A3, a Cysteine-Rich Calcium-Binding Protein, in Developing Hair Follicle
- Disease causing homozygous variants in the human hairless gene
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- Bloom's syndrome–‐a first report from India
- (673) Seminoma in SRY-Negative 46, XX Testicular Disorder of Sex Development Presenting as Acute Abdomen: An Extremely Rare Case Report
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Unusual Presentation of Childhood Leukemia With Vaginal Bleeding: A Case Report
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes