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 *

110 related articles for article (PubMed ID: 7389735)

  • 1. The mild form of pseudoachondroplasia. Identity of the morphological and biochemical alterations of growth cartilage with those of typical pseudoachondroplasia.
    Maroteaux P; Stanescu R; Stanescu V; Fontaine G
    Eur J Pediatr; 1980 May; 133(3):227-31. PubMed ID: 7389735
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Severe pseudoachondroplasia with parental consanguinity.
    Young ID; Moore JR
    J Med Genet; 1985 Apr; 22(2):150-3. PubMed ID: 3989835
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Patient with double heterozygosity for achondroplasia and pseudoachondroplasia, with comments on these conditions and the relationship between pseudoachondroplasia and multiple epiphyseal dysplasia, Fairbank type.
    Langer LO; Schaefer GB; Wadsworth DT
    Am J Med Genet; 1993 Oct; 47(5):772-81. PubMed ID: 8267011
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Gel electrophoretic studies on proteoglycans and collagen of abnormal human growth cartilage: proteoglycan abnormalities in pseudoachondroplasia and in Kniest's disease.
    Stanescu V; Maroteaux P
    Pediatr Res; 1975 Oct; 9(10):779-82. PubMed ID: 127160
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The biochemical defect of pseudoachondroplasia.
    Stanescu V; Maroteaux P; Stanescu R
    Eur J Pediatr; 1982 May; 138(3):221-5. PubMed ID: 7117284
    [No Abstract]   [Full Text] [Related]  

  • 6. Homozygous achondroplasia: morphologic and biochemical study of cartilage.
    Stanescu R; Stanescu V; Maroteaux P
    Am J Med Genet; 1990 Nov; 37(3):412-21. PubMed ID: 2260574
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The congenitally malformed. 13. Achondroplastic dwarfism; diagnosis and management.
    Shepard TH; Graham CB
    Northwest Med; 1967 May; 66(5):451-6. PubMed ID: 5623812
    [No Abstract]   [Full Text] [Related]  

  • 8. A large family with features of pseudoachondroplasia and multiple epiphyseal dysplasia: exclusion of seven candidate gene loci that encode proteins of the cartilage extracellular matrix.
    Rimoin DL; Rasmussen IM; Briggs MD; Roughley PJ; Gruber HE; Warman ML; Olsen BR; Hsia YE; Yuen J; Reinker K
    Hum Genet; 1994 Mar; 93(3):236-42. PubMed ID: 7907311
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pseudoachondroplasia: clinical diagnosis at different ages and comparison of autosomal dominant and recessive types. A review of 32 patients (26 kindreds).
    Wynne-Davies R; Hall CM; Young ID
    J Med Genet; 1986 Oct; 23(5):425-34. PubMed ID: 3783619
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypochondrogenesis.
    Maroteaux P; Stanescu V; Stanescu R
    Eur J Pediatr; 1983 Oct; 141(1):14-22. PubMed ID: 6641761
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Morphological and biochemical study of growth cartilage in osteochondrodysplasias].
    Stanescu V; Stanescu R; Maroteaux P
    Arch Fr Pediatr; 1977 Mar; 34 Suppl 1():I-LXXX. PubMed ID: 70194
    [No Abstract]   [Full Text] [Related]  

  • 12. Multiple epiphyseal dysplasia, Fairbank type: morphologic and biochemical study of cartilage.
    Stanescu R; Stanescu V; Muriel MP; Maroteaux P
    Am J Med Genet; 1993 Feb; 45(4):501-7. PubMed ID: 8465858
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pseudoachondroplasia: biochemical and histochemical studies of cartilage.
    Pedrini-Mille A; Maynard JA; Pedrini VA
    J Bone Joint Surg Am; 1984 Dec; 66(9):1408-14. PubMed ID: 6438109
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A special form of dominant spondylo-epiphyseal dysplasia (author's transl)]].
    Stanescu V; Stanescu R; Maroteaux P
    Arch Fr Pediatr; 1981 Dec; 38 Suppl 1():843-6. PubMed ID: 6800335
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A unique rough surfaced endoplasmic reticulum inclusion in pseudoachondroplasia.
    Maynard JA; Cooper RR; Ponseti IV
    Lab Invest; 1972 Jan; 26(1):40-4. PubMed ID: 4333078
    [No Abstract]   [Full Text] [Related]  

  • 16. Pseudoachondroplastic dysplasia: five cases representing clinical, roentgenographic and histologic heterogeneity.
    Cranley RE; Williams BR; Kopits SE; Dorst JP
    Birth Defects Orig Artic Ser; 1975; 11(6):205-15. PubMed ID: 172165
    [No Abstract]   [Full Text] [Related]  

  • 17. Pseudoachondroplasia.
    Hall JG
    Birth Defects Orig Artic Ser; 1975; 11(6):187-202. PubMed ID: 1201340
    [No Abstract]   [Full Text] [Related]  

  • 18. Pathogenesis of pseudoachondroplasia and diastrophic dysplasia.
    Stanescu V; Stanescu R; Maroteaux P
    Prog Clin Biol Res; 1982; 104():385-94. PubMed ID: 6298815
    [No Abstract]   [Full Text] [Related]  

  • 19. Identification of two novel mutations in the COMP gene in six families with pseudoachondroplasia.
    Yu WJ; Zhang Z; He JW; Fu WZ; Wang C; Zhang ZL
    Mol Med Rep; 2016 Sep; 14(3):2180-6. PubMed ID: 27432013
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pseudoachondroplasia: a case report.
    Radlović V; Smoljanić Z; Radlović N; Jakovljević M; Leković Z; Ducić S; Pavićević P
    Srp Arh Celok Lek; 2013; 141(9-10):676-9. PubMed ID: 24364233
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.