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    Research 31–60 of 1000+

    1. Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis Bioinformation · 2012 · 3 citations
    2. Hypertrichosis in Childhood Turkish Journal of Dermatology · 2018 · 1 citations
    3. Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa International journal of physiology · 2023
    4. A rare clinical image of hypertrichosis (Werewolf syndrome) ˜The œPan African medical journal · 2022
    5. Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin International Journal of Dermatology · 2009 · 20 citations
    6. Hereditary, Congenital, and Acquired Alopecias Elsevier eBooks · 2006 · 1 citations
    7. Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review Human Genomics · 2025
    8. Hereditary, Congenital, and Acquired Alopecias Elsevier eBooks · 2016
    9. Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors Dermatologic Therapy · 2022
    10. Congenital erythropoietic porphyria five years observation with standard treatment: a case report Oxford medical case reports · 2024
    11. Hirsutism and Hypertrichosis 2023
    12. Successful use of topical minoxidil in the treatment of hypotrichosis associated with desmoplakin mutations Pediatric dermatology · 2019 · 1 citations
    13. Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype Clinical Genetics · 2008 · 55 citations
    14. Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis Journal of dermatology · 2020 · 1 citations
    15. Congenital and Hereditary Skin Diseases 2018
    16. Congenital and Hereditary Skin Diseases 2018
    17. Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant Journal of Cosmetic Dermatology · 2025
    18. Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis 2022 · 6 citations
    19. A new type of pachyonychia congenita. PubMed · 2001 · 10 citations
    20. Cantú Syndrome Is Caused by Mutations in ABCC9 The American Journal of Human Genetics · 2012 · 148 citations
    21. A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22) Clinical Genetics · 1998 · 28 citations
    22. Cholesterol homeostasis: Links to hair follicle biology and hair disorders Experimental Dermatology · 2019 · 25 citations
    23. 农民致富的领路人——记“省青年星火带头人标兵”叶明 福建农业 · 2004
    24. Coat Problems 2021
    25. Disorders of hair in children Current Paediatrics · 2003
    26. Office Diagnosis of Hair Shaft Defects Seminars in cutaneous medicine and surgery · 2006 · 33 citations
    27. Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice PLOS genetics · 2020 · 23 citations
    28. A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions Human Genetics · 2019 · 10 citations
    29. Genetics of Alopecia Encyclopedia of Life Sciences · 2012
    30. A clinician's approach to canine alopecia Companion Animal · 2010