BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 6212507)

  • 21. A family with concurrent mesomelic shortening and hereditary nephritis.
    Funderburk SJ; Smith L; Falk RE; Bergstein JM; Winter H
    Birth Defects Orig Artic Ser; 1976; 12(6):47-61. PubMed ID: 788812
    [No Abstract]   [Full Text] [Related]  

  • 22. Two female siblings from Turkey with Langer mesomelic dysplasia (homozygous Leri-Weill dyschondrosteosis syndrome).
    Balci S; Zafer Y; Unsal M
    Turk J Pediatr; 1999; 41(4):531-9. PubMed ID: 10770125
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Stenosis of the lumbar spinal canal and dolichophalangy in a case of dyschondrosteosis (author's transl)].
    Leone G
    Radiol Med; 1979 Dec; 65(12):905-12. PubMed ID: 554217
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Leri-Weill's dyschondrosteosis].
    Muzzo S; Castillo C; Burrows R
    Rev Chil Pediatr; 1985; 56(3):184-7. PubMed ID: 4095311
    [No Abstract]   [Full Text] [Related]  

  • 25. Micromelic dwarfism--humerus, femur and tibia type.
    Al-Gazali LI; Bakir M; Hamid Z; Nath D; Haas D
    Clin Dysmorphol; 2001 Jan; 10(1):24-8. PubMed ID: 11152143
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Dyschondrosteosis and Madelung's deformity. Report of three kindreds and review of the literature.
    Beals RK; Lovrien EW
    Clin Orthop Relat Res; 1976 May; (116):24-8. PubMed ID: 1277646
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Madelung's deformity: observations in 17 patients.
    Felman AH; Kirkpatrick JA
    Radiology; 1969 Nov; 93(5):1037-42. PubMed ID: 5350668
    [No Abstract]   [Full Text] [Related]  

  • 29. Madelung's disease of the wrist and dyschondrosteosis.
    Golding JS; Blackburne JS
    J Bone Joint Surg Br; 1976 Aug; 58(3):350-2. PubMed ID: 956255
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [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]  

  • 31. Chondrodystrophic dwarfism and multiple malformations in two sisters.
    Pazzaglia UE; Pedrotti L; Beluffi G; Ceciliani L
    Pediatr Radiol; 1988; 19(1):41-4. PubMed ID: 3222061
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A case of dyschondrosteosis from Roman Britain.
    Waldron HA
    J Med Genet; 2000 Oct; 37(10):E27. PubMed ID: 11015459
    [No Abstract]   [Full Text] [Related]  

  • 33. Father to son transmission in metaphyseal chondrodysplasia mimicking vitamin D resistant rickets.
    Held KR; Riebel T; Schaefer E
    Prog Clin Biol Res; 1982; 104():143-8. PubMed ID: 6298812
    [No Abstract]   [Full Text] [Related]  

  • 34. [Mandelung's deformity: manifastation of dyschondrosteosis].
    Holenstein P; Buchs P
    Z Orthop Ihre Grenzgeb; 1967 Apr; 102(4):585-94. PubMed ID: 4233025
    [No Abstract]   [Full Text] [Related]  

  • 35. Picture of the month. Dyschondrosteosis (Leri-Weil syndrome, Leri's pleonostenosis).
    Rezvani I; Sharma RK; Collipp PJ
    Am J Dis Child; 1971 Nov; 122(5):429-30. PubMed ID: 5129533
    [No Abstract]   [Full Text] [Related]  

  • 36. [Differential diagnosis of Madelung's deformity: Léri-Weill syndrome].
    Ahmadi A; Zilch H
    Handchir Mikrochir Plast Chir; 1987 Nov; 19(6):315-7. PubMed ID: 3692340
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Radiographic patterns of dyschondrosteosis. (Leri-Weill disease).
    Hoeffel JC; Brauer B; Jimenez J; Hoeffel F
    Radiol Clin Biol; 1973; 42(5):366-72. PubMed ID: 4745065
    [No Abstract]   [Full Text] [Related]  

  • 38. Complete SHOX deficiency causes Langer mesomelic dysplasia.
    Zinn AR; Wei F; Zhang L; Elder FF; Scott CI; Marttila P; Ross JL
    Am J Med Genet; 2002 Jun; 110(2):158-63. PubMed ID: 12116254
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Probable homozygosity for the dyschondrosteosis genes.
    Espiritu CE; Chen H; Woolley PV
    Birth Defects Orig Artic Ser; 1975; 11(6):127-32. PubMed ID: 1201337
    [No Abstract]   [Full Text] [Related]  

  • 40. Isolated mesomelic shortening of the forearm in father and daughter: a new entity in the group of mesomelic dysplasias.
    Fryns JP; Hofkens G; Fabry G; van den Berghe H
    Clin Genet; 1988 Jan; 33(1):57-9. PubMed ID: 3342548
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.