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Journal Abstract Search

130 related items for PubMed ID: 3785882

  • 1. Ciliary and superciliary hypotrichosis. A distinct autosomal dominant trait.
    García-Esquivel L, Hernández A, Reynoso MC, Fragoso R, Villar-Calvo VM, Soto F, Cantú JM.
    Ophthalmic Paediatr Genet; 1986 Aug; 7(2):77-9. PubMed ID: 3785882
    [Abstract] [Full Text] [Related]

  • 2. Hereditary ciliary and superciliary hypotrichosis of a dominant character.
    URRETS-ZAVALIA A, JIMENEZ ES.
    Br J Ophthalmol; 1958 Nov; 42(11):694-6. PubMed ID: 13596561
    [No Abstract] [Full Text] [Related]

  • 3. Hypotrichosis with spondyloepimetaphyseal dysplasia in three generations: a new autosomal dominant syndrome.
    Whyte MP, Petersen DJ, McAlister WH.
    Am J Med Genet; 1990 Jul; 36(3):288-91. PubMed ID: 2363424
    [Abstract] [Full Text] [Related]

  • 4. Non-syndromic hypotrichosis: A report of two novel variants in the LSS gene.
    El Hakim J, Mehawej C, Chouery E, Megarbane A, El-Feghaly J, El Khoury J.
    Pediatr Dermatol; 2023 Jul; 40(5):960-961. PubMed ID: 37029088
    [Abstract] [Full Text] [Related]

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  • 6. Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia.
    Barrón-Hernández YL, Tosti A.
    Expert Opin Investig Drugs; 2017 Apr; 26(4):515-522. PubMed ID: 28264599
    [Abstract] [Full Text] [Related]

  • 7. [ON A FAMILY WITH THE RECESSIVE TRAIT OF WOOLLY HAIR, HYPOTRICHOSIS AND OTHER ANOMALIES].
    SALAMON T.
    Hautarzt; 1963 Dec; 14():540-4. PubMed ID: 14113527
    [No Abstract] [Full Text] [Related]

  • 8. Hereditary hypotrichosis simplex of the scalp.
    Kohn G, Metzker A.
    Clin Genet; 1987 Aug; 32(2):120-4. PubMed ID: 3652491
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  • 9. Atrichias and hypotrichoses: a brief review with description of a recessive atrichia in two brothers.
    Pinheiro M, Freire-Maia N.
    Hum Hered; 1985 Aug; 35(1):53-5. PubMed ID: 3972425
    [No Abstract] [Full Text] [Related]

  • 10. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Spiegl B, Hundeiker M.
    Fortschr Med; 1979 Nov 22; 97(44):2018-22. PubMed ID: 511082
    [Abstract] [Full Text] [Related]

  • 11. Hereditary hypotrichosis simplex of the scalp. Evidence for autosomal dominant inheritance.
    Toribio J, Quiñones PA.
    Br J Dermatol; 1974 Dec 22; 91(6):687-96. PubMed ID: 4141628
    [No Abstract] [Full Text] [Related]

  • 12. An autosomal dominant form of hereditary hypotrichosis simplex maps to 18p11.32-p11.23 in an Italian family.
    Baumer A, Belli S, Trüeb RM, Schinzel A.
    Eur J Hum Genet; 2000 Jun 22; 8(6):443-8. PubMed ID: 10878665
    [Abstract] [Full Text] [Related]

  • 13. Almost complete absence of the scalp and body hair in association with oligodontia and zygodactylous palmar triradii.
    Atasua M, Dumlu A, Ozbayrak S.
    Clin Dysmorphol; 2001 Oct 22; 10(4):269-72. PubMed ID: 11666001
    [Abstract] [Full Text] [Related]

  • 14. Hereditary hypotrichosis simplex of the scalp.
    Rodríguez Díaz E, Fernández Blasco G, Martín Pascual A, Armijo M.
    Dermatology; 1995 Oct 22; 191(2):139-41. PubMed ID: 8520061
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  • 16. Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance.
    Artlich A, Schwinger E, Meinecke P.
    Clin Dysmorphol; 1992 Jul 22; 1(3):157-60. PubMed ID: 1342863
    [Abstract] [Full Text] [Related]

  • 17. Incontinentia pigmenti. A four-generation study.
    Wiklund DA, Weston WL.
    Arch Dermatol; 1980 Jun 22; 116(6):701-3. PubMed ID: 7377807
    [Abstract] [Full Text] [Related]

  • 18. Hereditary hypotrichosis and localized morphea: a new clinical entity.
    Kulin P, Sybert VP.
    Pediatr Dermatol; 1986 Sep 22; 3(4):333-8. PubMed ID: 3774654
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  • 20. Very long eyelashes, long eyebrows, sparse hair, and mental retardation in two unrelated boys: An atypical form of Oliver-McFarlane syndrome without retinal degeneration, or a new clinical entity?
    Kondoh T, Amamoto N, Hirota T, Kinoshita E, Moriuchi H, Matsumoto T, Shimono M, Kawakami A, Shirahata A.
    Am J Med Genet A; 2003 Jul 30; 120A(3):437-8. PubMed ID: 12838570
    [No Abstract] [Full Text] [Related]

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