Search
for
Sort by
Research 661–690 of 1000+
- The Naked (N) Mutation, Chromosome 15
- Rates of polycystic ovary syndrome (PCOS) symptoms in relatives of patients with PCOS
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Research Snippets
- Hair Shaft Dysplasias
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions
- Alopecia X em cães: revisão
- Monilethrix
- [Netherton's syndrome in two sisters].
- P‐35 Nonlethal junctional epidermolysis bullosa in a dog
- [Anejaculation caused by haemosiderosis: male infertility in hereditary haemochromatosis].
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Hair Loss in Children
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Hair and nail disorders of childhood
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- Disorders of the Hair and Nails
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- AYURVEDIC COSMETOLOGY APPROACHES TO PREMATURE HAIR GREYING (AKĀLAPĀLITYA): A LITERATURE REVIEW
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Disorders of hair growth : diagnosis and treatment
- Predictive Modeling of Hair Fall using Random Forest Algorithms
- How Do You Treat Premature Hair Loss in Women in Your Practice
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Editorial: Vitamin D 1α-Hydroxylase Knockout Mice as a Hereditary Rickets Animal Model
- Androgеnеtic Alopеcia Pathogеnеsis, Diagnosis, and Trеatmеnt
- Androgenic alopecia and its association with metabolic syndrome
- Genetics Poly Cystic Ovary Syndrome