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Research 691–720 of 1000+
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Is polycystic ovary syndrome a sexual conflict? A review
- Patologías dermatológicas de origen nutricional en los pequeños animales: una revisión
- Congenital Adrenal Hyperplasia
- Inborn Errors of Biotin Metabolism
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Disorders of Hair Pigmentation
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Female Androgenetic Alopecia: A Separate Entity
- Senescence-accelerated Mouse (SAM): With Special Reference to Development and Pathobiological Phenotypes
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Acne-Associated Syndromes
- Inflammation in androgenetic alopecia and hair loss: linking neurosciences-endocrinology-dermatology
- Alopecia and its medical management
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- The endocrinology of baldness
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- Acknowledging the Clinical Heterogeneity of Lupus Erythematosus
- Vaccines, adjuvants and autoimmunity
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Familial frontal fibrosing alopecia: A cross‐sectional study of 20 cases from nine families
- Why were Sardinians the shortest Europeans? A journey through genes, infections, nutrition, and sex