BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 675214)

  • 1. [Familial mesomelial dwarfism (Nievergelt syndrome)].
    Hess OM; Goebel NH; Streuli R
    Schweiz Med Wochenschr; 1978 Aug; 108(31):1202-6. PubMed ID: 675214
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Dominant mesomelic dysplasia, ankle, carpal, and tarsal synostosis type: a new autosomal dominant bone disorder.
    Kantaputra PN; Gorlin RJ; Langer LO
    Am J Med Genet; 1992 Dec; 44(6):730-7. PubMed ID: 1481840
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Mesomelic dwarfism (author's transl)].
    Kemperdick H; Janssen F; Lenz W
    Rofo; 1975 Nov; 123(5):450-4. PubMed ID: 128504
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New syndrome: autosomal dominant microcephaly and radio-ulnar synostosis.
    Giuffrè L; Corsello G; Giuffrè M; Piccione M; Albanese A
    Am J Med Genet; 1994 Jul; 51(3):266-9. PubMed ID: 8074157
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dominant mesomelic dwarfism of the hypoplastic tibia, radius type.
    Leroy JG; De Vos J; Timmermans J
    Clin Genet; 1975 Apr; 7(4):280-6. PubMed ID: 1126050
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mesomelic dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome?
    Petrella R; Ludman MD; Rabinowitz JG; Gilbert F; Hirschhorn K
    Am J Med Genet; 1990 Sep; 37(1):10-4. PubMed ID: 2240023
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Nievergelt syndrome (mesomelic dwarfism-type Nievergelt).
    Young LW; Wood BP
    Birth Defects Orig Artic Ser; 1974; 10(5):81-6. PubMed ID: 4469999
    [No Abstract]   [Full Text] [Related]  

  • 8. [Mesomelic dwarfism Langer type associated to mixed gonadal dysgenesis, whit cariotipe 46,XY/45 X (author's transl)].
    Ruíz Gómez MJ; Martínez González M; Machín Jiménez AR; Fernández Villahoz AL
    An Esp Pediatr; 1979 Dec; 12(12):897-904. PubMed ID: 533057
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Ulno-fibular dysplasia. An autosome-dominant hereditary micromesomelia resembling the Nievergelt syndrome].
    Reinhardt K; Pfeiffer RA
    Fortschr Geb Rontgenstr Nuklearmed; 1967 Sep; 107(3):379-91. PubMed ID: 5626375
    [No Abstract]   [Full Text] [Related]  

  • 10. [Acro-coxo-mesomelic dwarfism: a new variety of autosomal recessive dwarfism].
    Plauchu H; Maisonneuve D; Floret D
    Ann Genet; 1984; 27(2):83-7. PubMed ID: 6331794
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.
    Fujimoto M; Kantaputra PN; Ikegawa S; Fukushima Y; Sonta S; Matsuo M; Ishida T; Matsumoto T; Kondo S; Tomita H; Deng HX; D'urso M; Rinaldi MM; Ventruto V; Takagi T; Nakamura Y; Niikawa N
    J Hum Genet; 1998; 43(1):32-6. PubMed ID: 9609995
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Mesomelic dwarfism of the Langer type as a homozygous form of dyschondrosteosis (author's transl)].
    Kemperdick H; Majewski F
    Rofo; 1982 May; 136(5):583-7. PubMed ID: 6212507
    [No Abstract]   [Full Text] [Related]  

  • 13. Familial infantile cortical hyperostosis in a large Canadian family.
    Maclachlan AK; Gerrard JW; Houston CS; Ives EJ
    Can Med Assoc J; 1984 May; 130(9):1172-4. PubMed ID: 6370402
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Congenital skeletal limb deficiencies. Examples and their treatment].
    Seyhan F; Ahiskali G
    Turk Tip Cemiy Mecm; 1972 Nov; 38(11):481-8. PubMed ID: 4668355
    [No Abstract]   [Full Text] [Related]  

  • 15. [Fibular dimelia].
    Sułko J
    Chir Narzadow Ruchu Ortop Pol; 2009; 74(1):18-21. PubMed ID: 19514474
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dyschondrosteosis (mesomelic dwarfism)--a family study.
    Carter AR; Currey HL
    Br J Radiol; 1974 Oct; 47(562):634-40. PubMed ID: 4433973
    [No Abstract]   [Full Text] [Related]  

  • 17. [Genetic counseling in defect abnormalities of the extremities (proceedings)].
    Lenz W
    Z Orthop Ihre Grenzgeb; 1978 Aug; 116(4):558-60. PubMed ID: 212892
    [No Abstract]   [Full Text] [Related]  

  • 18. [Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome].
    Stoll C; Roth MP; Levy JM
    J Genet Hum; 1980 Sep; 28(3):299-304. PubMed ID: 7463030
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Triangular tibia with fibular aplasia associated with a microdeletion on 2q11.2 encompassing LAF4.
    Steichen-Gersdorf E; Gassner I; Superti-Furga A; Ullmann R; Stricker S; Klopocki E; Mundlos S
    Clin Genet; 2008 Dec; 74(6):560-5. PubMed ID: 18616733
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The WT syndrome--a "new" autosomal dominant pleiotropic trait of radial/ulnar hypoplasia with high risk of bone marrow failure and/or leukemia.
    Gonzalez CH; Durkin-Stamm MV; Geimer NF; Shahidi NT; Schilling RF; Rubira F; Opitz JM
    Birth Defects Orig Artic Ser; 1977; 13(3B):31-8. PubMed ID: 890097
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.