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 *

129 related articles for article (PubMed ID: 788812)

  • 21. Radiographic diagnosis of neonatal short-limbed dwarfism.
    Saldino RM
    Med Radiogr Photogr; 1973; 49(3):61-95. PubMed ID: 4775541
    [No Abstract]   [Full Text] [Related]  

  • 22. Metatropic dysplasia is associated with increased fracture risk.
    Bober MB; Duker AL; Carney M; Ditro CP; Rogers K; Mackenzie WG
    Am J Med Genet A; 2016 May; 170A(5):1373-6. PubMed ID: 26823048
    [No Abstract]   [Full Text] [Related]  

  • 23. The lethal chondrodysplasias.
    Maroteaux P; Stanescu V; Stanescu R
    Clin Orthop Relat Res; 1976; (114):31-45. PubMed ID: 1261128
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Mesomelic dwarfism. Pronounced form in a female infant of a father with dyschondrosteosis and a mother with Madelung's deformity].
    Gugliantini P; Scapaticci A
    Radiol Med; 1978 Apr; 64(4):433-44. PubMed ID: 704970
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Angiographic study of hereditary nephritis (Alport's syndrome).
    Demetropoulos KC; Hoskins P; Rapp R
    Radiology; 1973 Sep; 108(3):539-40. PubMed ID: 4723654
    [No Abstract]   [Full Text] [Related]  

  • 26. Metatropic dwarfism, the Kniest syndrome and the pseudoachondroplastic dysplasias.
    Rimoin DL; Siggers DC; Lachman RS; Silberberg R
    Clin Orthop Relat Res; 1976; (114):70-82. PubMed ID: 177239
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [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]  

  • 28. Autosomal recessive inheritance in the mesomelic dwarfism of Campailla and Martinelli.
    Beighton P
    Clin Genet; 1974; 5(4):363-7. PubMed ID: 4850715
    [No Abstract]   [Full Text] [Related]  

  • 29. [Roentgenosemeiotics of hereditary nephritis in children].
    Bosin VIu; Ignatova MS; Fokeeva VV; Skripkina LA; Degtiareva EM
    Pediatriia; 1979 Feb; (2):25-9. PubMed ID: 450575
    [No Abstract]   [Full Text] [Related]  

  • 30. [Hereditary nephritis (Alport's syndrome). Description of a family].
    Marcen Letosa R; Fdez Alonso J; Quereda Rguez navarro C; López Checa F; Castilla Jiménez J; Rodríguez Algarra G; Maceira Cruz B; Pereira Palomo P; Mateos Aguilar J
    Rev Clin Esp; 1977 Nov; 147(3):291-6. PubMed ID: 605240
    [No Abstract]   [Full Text] [Related]  

  • 31. Hereditary nephritis and deafness. Report of a family.
    Shani M; Fine LG
    Isr J Med Sci; 1970; 6(4):544-8. PubMed ID: 5472337
    [No Abstract]   [Full Text] [Related]  

  • 32. [Hereditary systemic diseases of the skeleton].
    Spranger J
    Radiologe; 1973 Apr; 13(4):141-6. PubMed ID: 4197800
    [No Abstract]   [Full Text] [Related]  

  • 33. Diastrophic dwarfism.
    Cisárik F; Kostra M; Grossmann J; Kacejova M
    Radiol Diagn (Berl); 1980; 21(6):795-803. PubMed ID: 7244203
    [No Abstract]   [Full Text] [Related]  

  • 34. 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]  

  • 35. Bilateral hereditary micro-epiphyseal dysplasia: further delineation of the phenotype with 40 years follow-up.
    Mostert AK; Jansen BR; Dijkstra PF; Wesby-van Swaay E; van Horn JR; Heutink P; Lindhout D
    Int Orthop; 2002; 26(3):188-93. PubMed ID: 12073115
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Familial Blomstrand chondrodysplasia with advanced skeletal maturation: further delineation.
    Loshkajian A; Roume J; Stanescu V; Delezoide AL; Stampf F; Maroteaux P
    Am J Med Genet; 1997 Aug; 71(3):283-8. PubMed ID: 9268097
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Kniest's dysplasia].
    Tscherninkov S; Alexandrov A
    Radiol Diagn (Berl); 1990; 31(3):267-71. PubMed ID: 2367633
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Lethal forms of chondrodysplastic dwarfism.
    Curran JP; Sigmon BA; Opitz JM
    Pediatrics; 1974 Jan; 53(1):76-85. PubMed ID: 4809196
    [No Abstract]   [Full Text] [Related]  

  • 39. Upington disease: a familial dyschondroplasia.
    Schweitzer G; Jones B; Timme A
    S Afr Med J; 1971 Sep; 45(36):994-1000. PubMed ID: 5316541
    [No Abstract]   [Full Text] [Related]  

  • 40. Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.
    Mutesa L; Vanbellinghen JF; Hellin AC; Segers K; Jamar M; Pierquin G; Bours V
    Genet Couns; 2009; 20(1):9-17. PubMed ID: 19400538
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.