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 *

183 related articles for article (PubMed ID: 7025944)

  • 1. Congenital abnormalities of the limbs.
    Fixsen J
    Br J Hosp Med; 1981 Sep; 26(3):194, 196-7, 200-3. PubMed ID: 7025944
    [No Abstract]   [Full Text] [Related]  

  • 2. Diagnosis and treatment of congenital deformities of the musculoskeletal system in the newborn and the infant.
    Tachdjian MO
    Pediatr Clin North Am; 1967 May; 14(2):307-58. PubMed ID: 5337113
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. [Possible errors in ultrasound hip imaging in patients with osteogenesis imperfecta].
    Hahn H; Färber D; Stern H; Pontz BF
    Ultraschall Med; 1994 Dec; 15(6):282-5. PubMed ID: 7846504
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Osteogenesis imperfecta type 1 with an incidental finding of bilateral radioulnar synostosis.
    Apperley LJ; Richmond S; Ramakrishnan R; Balasubramanian M
    Clin Dysmorphol; 2020 Jul; 29(3):155-157. PubMed ID: 32282353
    [No Abstract]   [Full Text] [Related]  

  • 6. [Syndrome of caudal dysplasia].
    Mastella G
    Fracastoro; 1969; 62(1):95-102. PubMed ID: 5402916
    [No Abstract]   [Full Text] [Related]  

  • 7. [Radiusaplasia with T thrombocytopenia. A genetic syndrome].
    Haarmann M; Lenz W; Petersen D
    Ergeb Inn Med Kinderheilkd; 1975; 37():57-106. PubMed ID: 1157813
    [No Abstract]   [Full Text] [Related]  

  • 8. Dysmelia. A classification and a pattern of malformation in a group of congenital defects of the limbs.
    Henkel L; Willert HG
    J Bone Joint Surg Br; 1969 Aug; 51(3):399-414. PubMed ID: 5820783
    [No Abstract]   [Full Text] [Related]  

  • 9. The syndrome of multisynostotic osteodysgenesis with long-bone fractures.
    DeLozier CD; Antley RM; Williams R; Green N; Heller RM; Bixler D; Engel E
    Am J Med Genet; 1980; 7(3):391-403. PubMed ID: 7468663
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [Congenital radio-ulnar synostosis].
    Rodríguez García L; Armendáriz Mekjavich M; Urzainki Martínez F; Otero Arévalo E; García Mata S
    An Esp Pediatr; 2002 Jan; 56(1):75-6. PubMed ID: 11792254
    [No Abstract]   [Full Text] [Related]  

  • 12. Congenital disorders of the extremities.
    Mandell GA; Harcke HT; Kumar SJ
    Top Magn Reson Imaging; 1991 Dec; 4(1):1-20. PubMed ID: 1764254
    [No Abstract]   [Full Text] [Related]  

  • 13. [49,XXXXY syndrome in a 5-year-old boy].
    Wiśniewski L; Krajewska-Walasek M; Lech H; Mospinek M
    Pediatr Pol; 1980 Jan; 55(1):81-6. PubMed ID: 7189276
    [No Abstract]   [Full Text] [Related]  

  • 14. Congenital postural deformity association.
    Pazonyi I; Kun A; Czeizel A
    Acta Paediatr Acad Sci Hung; 1982; 23(4):431-45. PubMed ID: 7170954
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Congenital extension stiffness of the knee].
    Stranák V; Palme E
    Beitr Orthop Traumatol; 1968 Oct; 15(10):571-2. PubMed ID: 5734738
    [No Abstract]   [Full Text] [Related]  

  • 16. [Cranio-carpo-tarsal dysplasia syndrome (Freeman-Sheldon syndrome, whistling face syndrome)].
    Träger D
    Z Orthop Ihre Grenzgeb; 1987; 125(1):106-7. PubMed ID: 3577337
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Osteogenesis imperfecta and congenital dislocation of the hip.
    Williams LH
    BMJ; 1992 Oct; 305(6858):885. PubMed ID: 1422410
    [No Abstract]   [Full Text] [Related]  

  • 18. Osteogenesis imperfecta and congenital dislocation of the hip.
    Mellon AF
    BMJ; 1992 Oct; 305(6858):885. PubMed ID: 1422409
    [No Abstract]   [Full Text] [Related]  

  • 19. [A case of osteogenesis imperfecta of the Vrolik type].
    Pătrună F
    Rev Pediatr Obstet Ginecol Pediatr; 1981; 30(3):279-81. PubMed ID: 6800019
    [No Abstract]   [Full Text] [Related]  

  • 20. Radioulnar synostosis in Williams-Beuren syndrome: a component manifestation.
    Pankau R; Gosch A; Wessel A
    Am J Med Genet; 1993 Mar; 45(6):783. PubMed ID: 8456863
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.