These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

145 related articles for article (PubMed ID: 4206841)

  • 1. The Winchester syndrome: a nonlysosomal connective tissue disease.
    Hollister DW; Rimoin DL; Lachman RS; Cohen AH; Reed WB; Westin GW
    J Pediatr; 1974 May; 84(5):701-9. PubMed ID: 4206841
    [No Abstract]   [Full Text] [Related]  

  • 2. The Winchester syndrome: clinical, radiographic and pathologic studies.
    Hollister DW; Rimoin DL; Lachman RS; Westin GW; Cohen AH
    Birth Defects Orig Artic Ser; 1974; 10(10):89-100. PubMed ID: 4462644
    [No Abstract]   [Full Text] [Related]  

  • 3. The skin in the Winchester syndrome.
    Cohen AH; Hollister DW; Reed WB
    Arch Dermatol; 1975 Feb; 111(2):230-6. PubMed ID: 1115514
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Progressive multilayered banded skin in Winchester syndrome.
    Sidwell RU; Brueton LA; Grabczynska SA; Francis N; Staughton RC
    J Am Acad Dermatol; 2004 Feb; 50(2 Suppl):S53-6. PubMed ID: 14726867
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hurler/Scheie genetic compound (mucopolysaccharidosis IH/IS) in Japanese brothers.
    Kajii T; Matsuda I; Osawa T; Katsunuma H; Ichida T
    Clin Genet; 1974; 6(5):394-400. PubMed ID: 4373197
    [No Abstract]   [Full Text] [Related]  

  • 6. Heritable disorders of connective tissue.
    JAMA; 1973 Apr; 224(5 Suppl):774-6. PubMed ID: 4266956
    [No Abstract]   [Full Text] [Related]  

  • 7. Concordant metaphyseal dysostosis type Schmid in twins.
    Kajii T; Osawa T; Matsuda I; Sugai M
    Humangenetik; 1971; 13(2):151-6. PubMed ID: 5114668
    [No Abstract]   [Full Text] [Related]  

  • 8. The genetics of short stature.
    Scott CI
    Prog Med Genet; 1972; 8():243-99. PubMed ID: 4259833
    [No Abstract]   [Full Text] [Related]  

  • 9. [3 hereditary growth disorders].
    Perheentupa J
    Duodecim; 1972; 88(1):60-71. PubMed ID: 5013579
    [No Abstract]   [Full Text] [Related]  

  • 10. Collagen disorders and skeletal dysplasias.
    Bonaventure J; Cohen-Solal L; Maroteaux P
    Curr Opin Rheumatol; 1990 Feb; 2(1):38-43. PubMed ID: 2223453
    [No Abstract]   [Full Text] [Related]  

  • 11. A newly recognized syndrome of connective tissue dysplasia in siblings (previously described as a variant of Morquio disease).
    Spellacy E; Gibbs DA; Watts RW
    Q J Med; 1981; 50(200):377-415. PubMed ID: 6805033
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Study of congenital osteodystrophies. Considerations on 4 cases of Rathbun's hypophosphatasia and 7 unusual cases of rachitic osteodystrophy].
    Tirnoveanu G; Georgescu MI; Mitescu G
    Rev Med Chir Soc Med Nat Iasi; 1972; 16(3):667-72. PubMed ID: 5080559
    [No Abstract]   [Full Text] [Related]  

  • 13. Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxity.
    Bonaventure J; Stanescu R; Stanescu V; Allain JC; Muriel MP; Ginisty D; Maroteaux P
    Am J Med Genet; 1992 Dec; 44(6):738-53. PubMed ID: 1481841
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A syndrome of systemic hyalinosis, short-limb dwarfism and possible thymic dysplasia.
    Alfi OS; Heuser ET; Landing BH; Robinson RE; Nadler S; Donnell GN
    Birth Defects Orig Artic Ser; 1975; 11(5):57-62. PubMed ID: 56200
    [No Abstract]   [Full Text] [Related]  

  • 15. Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome.
    Evans BR; Mosig RA; Lobl M; Martignetti CR; Camacho C; Grum-Tokars V; Glucksman MJ; Martignetti JA
    Am J Hum Genet; 2012 Sep; 91(3):572-6. PubMed ID: 22922033
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Metacarpophalangeal pattern as well as length and proportions of the bones of the extremities in an infant with Robinow's syndrome II].
    Oliván Gonzalvo G; Sarriá Chueca A; Ventura Faci P; Pérez González JM; Bueno Sánchez M
    An Esp Pediatr; 1990 Jul; 33(1):82-4. PubMed ID: 2252297
    [No Abstract]   [Full Text] [Related]  

  • 17. [Current status of the physiology and new trends in the pathology of connective tissue. IV. Nosology and nosography of primary diffuse diseases of connective tissue].
    Lenzi L; Silva E
    Chir Organi Mov; 1968; 56(3):196-236. PubMed ID: 4245323
    [No Abstract]   [Full Text] [Related]  

  • 18. A constitutional disorder of connective tissue suggesting a defect in collagen biosynthesis.
    Meigel WN; Müller PK; Pontz BF; Sörensen N; Spranger J
    Klin Wochenschr; 1974 Oct; 52(19):906-12. PubMed ID: 4457717
    [No Abstract]   [Full Text] [Related]  

  • 19. [Hereditary bone dystrophy. Pyknodysostosis].
    Sada Moreno E; Martinez Lage JL; Vazquez Ajuria F; Jimenez Burkhardt A
    Rev Esp Estomatol; 1980; 28(6):331-6. PubMed ID: 6798645
    [No Abstract]   [Full Text] [Related]  

  • 20. The Kniest syndrome.
    Siggers CD; Rimoin DL; Dorst JP; Doty SB; Williams BR; Hollister DW; Silberberg R; Cranley RE; Kaufman RL; McKusick VA
    Birth Defects Orig Artic Ser; 1974; 10(9):193-208. PubMed ID: 4214536
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.