Search
for
Sort by
Research 301–330 of 1000+
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- KASUS RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA-MITIS YANG TERDIAGNOSIS PADA SAAT LANJUT USIA
- The Case | Bilateral kidney tumors and lung cysts
- Obesity and Polycystic Ovary Syndrome: Implications for Pathogenesis and Novel Management Strategies
- Genetic basis of polycystic ovary syndrome
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Australasian Society for Dermatology Research Meeting, May 2006
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review
- 5α Reductase Deficiency—a Rare Cause of Ambiguous Genitalia and Gender Dysphoria
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Identification and characterization of genes for skin and hair disorders
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- The genetics of hair shaft disorders
- Biotin and Acetazolamide for Treatment of an Unusual Child With Autism Plus Lack of Nail and Hair Growth
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient