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Research 211–240 of 1000+
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Congenital atrichia with papular lesions
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
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- A Newborn With Hair Loss
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- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- Woolly hair generalizado: caso clínico e revisão da literatura
- Reviewer #3 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Congenital Atrichia: A Case Report
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Tricotiodistrofia. Reporte de un caso
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Molecular Basis of Hereditary Hair Diseases
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Evaluation of hair structural abnormalities in children with different neurological diseases
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Clinical report of a Holstein's calf with ichthyosis.
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study