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Research 271–300 of 348
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Marie-unna hereditary hypotrichosis
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- The potential impact of melanosomal pH and metabolism on melanoma
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Transcriptomes reveal microRNAs and mRNAs in different photoperiods influencing cashmere growth in goat
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Androgen-associated and androgen-independent causes of alopecia and acne in women. Literature review
- Trailing the Path to Preventive Oncology
- Genome-wide association study reveals candidate genes associated with body weight and wool traits in Ordos fine-wool sheep
- PERBANDINGAN ARMS-PCR DAN ALLELE-SPECIFIC PCR DALAM OPTIMASI GENOTIPING SNP rs1998076
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Novel Insights into TSC22D Family Genes in Metabolic Diseases and Cancer
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- A Rare Case of Generalized Staphylococcal Dermatitis in European Bison
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development