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Research 151–180 of 1000+
- Fertility and Sterility Vol 101 No 4, April 2014
- Isolation and Characterization of Cutaneous Epithelial Stem Cells
- Analysis of Various Factors Responsible for Hair Loss and Awareness Level in Delhi and the National Capital Region of India
- PA33 When bones speak through nails: insights from a paediatric case series
- Trichothiodystrophy: Current Concepts
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Nonclassic congenital adrenal hyperplasia
- EVALUATION OF HAIR GROWTH PROMOTING POTENTIAL OF DURDHURADI TAILA THROUGH MODULATION OF 5Α-REDUCTASE GENE EXPRESSION
- Interplay between fibroblast growth factor 9 (FGF9) and CD44 underlies 46,XY disorders of sex development in Kruppel‐like factor 1 (KLF‐1)‐E325K‐associated congenital dyserythropoietic anaemia (CDA‐IV)
- A clinical case of CNOT3 syndrome in a 10-year-old girl
- Research progress on the pathogenesis of androgenetic alopecia
- British Society for Dermatopathology
- Forensic DNA phenotyping: the need for proportionate regulation and judicial clarity in law enforcement
- HAIR LOSS IN WOMEN
- Forensic DNA Phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Diagnosis dan Tata Laksana Graves’ Disease
- Benefits vs. harms of using Mega Hair
- Monilethrix – Case report of a rare disease
- This Month in the Journal
- КЛІНІЧНІ ФЕНОТИПИ ВИСОКОГО РИЗИКУ НАЯВНОСТІ ПЕРВИННИХ МІТОХОНДРІАЛЬНИХ ЦИТОПАТІЙ (частина 2)
- Female pattern hair loss: Clinico-laboratory findings and trichoscopy depending on disease severity
- Hypotrichosis with juvenile macular dystrophy
- Lifestyle Risk Factors in Male Androgenetic Alopecia: A Cross-sectional Study
- Molecular characterisation of keratin-associated protein-7 (KRTAP7) gene for hair quality in Indian Dromedary Camel
- Introduction pages
- Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of β-catenin in mice
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Detection of mutations in the CYP21A2 gene: genotype-phenotype correlation in Slovenian couples with conceiving problems
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis