BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 3823961)

  • 21. Mesomelic dwarfism as the homozygous expression of dyschondrosteosis.
    Espiritu C; Chen H; Woolley PV
    Am J Dis Child; 1975 Mar; 129(3):375-7. PubMed ID: 1121969
    [No Abstract]   [Full Text] [Related]  

  • 22. A case with spondylo-metaphyseal dysplasia type A4.
    Percin EF; Tukenmez M; Percin S
    Genet Couns; 2004; 15(3):363-9. PubMed ID: 15517830
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical, radiographic, and pathologic abnormalities in dogs with multiple epiphyseal dysplasia: 19 cases (1991-2005).
    Rørvik AM; Teige J; Ottesen N; Lingaas F
    J Am Vet Med Assoc; 2008 Aug; 233(4):600-6. PubMed ID: 18710316
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly).
    Lazalde B; Sánchez-Urbina R; Nuño-Arana I; Bitar WE; de Lourdes Ramírez-Dueñas M
    Am J Med Genet; 2000 Oct; 94(5):421-7. PubMed ID: 11050630
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Spondylometaphyseal dysplasia: further heterogeneity.
    Borochowitz Z; Berant M; Kristal H
    Skeletal Radiol; 1988; 17(3):181-6. PubMed ID: 3375844
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Autosomal dominant congenital epiphyseal dysplasia limited to the femoral heads.
    Hernández A; Nazara Z; Reynoso MC; Lizcano-Gil LA; Lopez R; Sarralde A; Fragoso R
    Genet Couns; 1996; 7(3):187-91. PubMed ID: 8897039
    [TBL] [Abstract][Full Text] [Related]  

  • 27. New autosomal dominant form of spondyloepiphyseal dysplasia presenting with atlanto-axial instability.
    Reardon W; Hall CM; Shaw DG; Kendall B; Hayward R; Winter RM
    Am J Med Genet; 1994 Oct; 52(4):432-7. PubMed ID: 7747755
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Van Buchem disease: surgical treatment of the mandible.
    Schendel SA
    Ann Plast Surg; 1988 May; 20(5):462-7. PubMed ID: 3377422
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Autosomal dominant osteosclerosis: report of a kindred.
    Curran AE; Pfeffle RC; Miller E
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 1999 May; 87(5):600-4. PubMed ID: 10348520
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritance.
    Hall CM; Elcioglu NH; MacDermot KD; Offiah AC; Winter RM
    J Med Genet; 2002 Sep; 39(9):666-70. PubMed ID: 12205110
    [No Abstract]   [Full Text] [Related]  

  • 31. [Autosomal recessive spondylometaphyseal dysplasia. Apropos of 3 familial cases].
    Meziane AO; Meziane A; Ksiyer M; Bennani-Smires C; Khalifa HH
    Ann Genet; 1987; 30(4):216-20. PubMed ID: 3501265
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Leri-Weill syndrome (dyschondrosteosis). Description of 2 clinical cases].
    Radetti G; Pasquino B; Munari E; Mengarda G
    Pediatr Med Chir; 1987; 9(3):367-70. PubMed ID: 3671136
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Pacman dysplasia: report of two affected sibs.
    Wilcox WR; Lucas BC; Loebel B; Bachman RP; Lachman RS; Rimoin DL
    Am J Med Genet; 1998 May; 77(4):272-6. PubMed ID: 9600734
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation.
    Rickels MR; Zhang X; Mumm S; Whyte MP
    J Bone Miner Res; 2005 May; 20(5):878-85. PubMed ID: 15824861
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family.
    Simsek S; Janssens K; Kwee ML; Van Hul W; Veenstra J; Netelenbos JC
    Osteoporos Int; 2005 Sep; 16(9):1167-70. PubMed ID: 15959620
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Progressive diaphyseal dysplasia (Camurati-Engelmann): radiographic follow-up and CT findings.
    Kaftori JK; Kleinhaus U; Naveh Y
    Radiology; 1987 Sep; 164(3):777-82. PubMed ID: 3615880
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Handigodu disease: a radiological study. A new variety of spondyloepi(meta)physeal dysplasia of the autosomal dominant type.
    Agarwal SS; Phadke SR; Phadke RV; Das SK; Singh GK; Sharma JP; Teotia SP; Saxena BN
    Skeletal Radiol; 1994 Nov; 23(8):611-9. PubMed ID: 7886470
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Autosomal dominant precocious osteoarthropathy due to a mutation of the cartilage oligomeric matrix protein (COMP) gene: further expansion of the phenotypic variations of COMP defects.
    Kawaji H; Nishimura G; Watanabe S; Mabuchi A; Ikeda T; Ohashi H; Sasaki A; Sano T; Ikegawa S
    Skeletal Radiol; 2002 Dec; 31(12):730-7. PubMed ID: 12483437
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Craniometaphyseal dysplasia associated with obstructive sleep apnoea syndrome.
    Mintz S; Velez I
    Dentomaxillofac Radiol; 2004 Jul; 33(4):262-6. PubMed ID: 15533982
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Infantile cortical hyperostosis.
    Frána L; Sekanina M
    Arch Dis Child; 1976 Aug; 51(8):589-95. PubMed ID: 786183
    [TBL] [Abstract][Full Text] [Related]  

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