BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 7159163)

  • 1. [Camptomelic dysplasia. A case of survival for more than 4 years].
    Noyal P; Vermeulin G; Hibon D; Meck JM
    Arch Fr Pediatr; 1982 Oct; 39(8):621-4. PubMed ID: 7159163
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sponastrime dysplasia: diagnostic criteria based on five new and six previously published cases.
    Langer LO; Beals RK; Scott CI
    Pediatr Radiol; 1997 May; 27(5):409-14. PubMed ID: 9133352
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Campomelic dysplasia. Further elucidation of a distinct entity.
    Hall BD; Spranger JW
    Am J Dis Child; 1980 Mar; 134(3):285-9. PubMed ID: 7361736
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Congenital familial dwarfism with cephaloskeletal dysplasia (Taybi-Linder syndrome)].
    Lavollay B; Faure C; Filipe G; Branca G; Huet de Barochez Y
    Arch Fr Pediatr; 1984 Jan; 41(1):57-60. PubMed ID: 6721654
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital familial dwarfism with cephalo-skeletal dysplasia.
    Thomas PS; Nevin NC
    Ann Radiol (Paris); 1976; 19(1):187-92. PubMed ID: 984702
    [No Abstract]   [Full Text] [Related]  

  • 6. Metaphyseal dysplasia, type Schmid.
    Beluffi G; Fiori P; Schifino A; Notarangelo LD; Giardini D; Bozzola M; Montanari C; Martini A
    Prog Clin Biol Res; 1982; 104():103-10. PubMed ID: 7163252
    [No Abstract]   [Full Text] [Related]  

  • 7. Dwarfism in the newborn: the nomenclature, radiological features and genetic significance.
    Cremin BJ; Beighton P
    Br J Radiol; 1974 Feb; 47(554):77-93. PubMed ID: 4206212
    [No Abstract]   [Full Text] [Related]  

  • 8. Kyphomelic dysplasia: clinical and radiologic long-term follow-up of one case and review of the literature.
    Pallotta R; Ehresmann T; Roggini M; Fusilli P
    Radiology; 1999 Sep; 212(3):847-52. PubMed ID: 10478256
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Kniest's disease, (a familial case)].
    Gnamey D; Farriaux JP; Fontaine G
    Arch Fr Pediatr; 1976 Feb; 33(2):143-51. PubMed ID: 973772
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial congenital micromelic dysplasia with dislocation of radius and distinct face: a new skeletal dysplasia syndrome.
    Borochowitz Z; Barak M; Hershkowitz S
    Am J Med Genet; 1991 Apr; 39(1):91-6. PubMed ID: 1867270
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An unusual bone dysplasia: parastremmatic dwarfism.
    Langer LO; Petersen D; Spranger J
    Am J Roentgenol Radium Ther Nucl Med; 1970 Nov; 110(3):550-60. PubMed ID: 4992387
    [No Abstract]   [Full Text] [Related]  

  • 12. Acromicric dysplasia and geleophysic dysplasia: similarities and differences.
    Hennekam RC; van Bever Y; Oorthuys JW
    Eur J Pediatr; 1996 Apr; 155(4):311-4. PubMed ID: 8777926
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hypochondroplasia: importance of radiological findings in the differential diagnosis of short statures of different origin].
    Iannaccone R; Tiberti AC
    Recenti Prog Med; 2001; 92(7-8):483-8. PubMed ID: 11475794
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The SPONASTRIME dysplasia: familial short-limb dwarfism with saddle nose, spinal alterations and metaphyseal striation. Report of 4 siblings.
    Fanconi S; Issler C; Giedion A; Prader A
    Helv Paediatr Acta; 1983 Aug; 38(3):267-80. PubMed ID: 6618893
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Camptomelic dysplasia associated with true hermaphroditism].
    Delgado A; Egües J; Molina M; Martínez Peñuela JM; Santolaya JM
    An Esp Pediatr; 1984 May; 20(8):792-9. PubMed ID: 6476626
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Radiological case of the month. Dyschondrosteosis (Leri-Weill Syndrome).
    Gwinn JL; Lee FA
    Am J Dis Child; 1972 Aug; 124(2):243-4. PubMed ID: 5052409
    [No Abstract]   [Full Text] [Related]  

  • 17. A new skeletal dysplasia syndrome with dwarfism, craniofacial anomalies, and unique radiographic findings.
    Jones KL; Jones KL; Miller K
    Am J Med Genet; 1986 Mar; 23(3):751-7. PubMed ID: 2420178
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dyggve-Melchior-Clausen syndrome: genetic studies and report of affected sibs.
    Toledo SP; Saldanha PH; Lamego C; Mourão PA; Dietrich CP; Mattar E
    Am J Med Genet; 1979; 4(3):255-61. PubMed ID: 117710
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Otopalatodigital syndrome. Apropos of 3 female cases].
    Plenier V; Delaire J; David A; Cohen JY
    Rev Stomatol Chir Maxillofac; 1983; 84(6):322-9. PubMed ID: 6583818
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Short rib-polydactyly syndrome, Majewski type.
    Chen H; Yang SS; Gonzalez E; Fowler M; Al Saadi A
    Am J Med Genet; 1980; 7(2):215-22. PubMed ID: 7468649
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.