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Research 30 of 159
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Rhombencephalosynapsis presenting antenatally with ventriculomegaly/hydrocephalus in a likely case of Gomez–López-Hernández syndrome
- Adverse effects of 5α-reductase inhibitors: What do we know, don’t know, and need to know?
- Molecular Genetics of Alopecias
- Abstract 22: Tafluprost, a Prostaglandin F2α Analog, Has Therapeutic Potential for Androgenic Alopecia through Modulation of Hair Cycle
- Alopecia in Association with Malignancy: A Review
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- <i>WNT10A</i> , dermatology and dentistry
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Biology and Genetics of Hair
- Inherited Disorders of the Hair
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Alopecia Areata with Renal Dysgenesis
- Fertility and Sterility Vol 101 No 4, April 2014
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Hair and Nail Relationship
- Rhamnose-mediated modulation of hair follicle growth: insights from chemical genomics
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- AAPS and PSRC 2016 Abstract Supplement
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex