BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

222 related articles for article (PubMed ID: 8929375)

  • 1. Radiographic findings in Shprintzen-Goldberg syndrome.
    Nishimura G; Nagai T
    Pediatr Radiol; 1996 Nov; 26(11):775-8. PubMed ID: 8929375
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Radiological changes of frontometaphyseal dysplasia in the neonate.
    Nishimura G; Takano H; Aihara T; Ohashi H; Fukushima Y; Satoh M
    Pediatr Radiol; 1995 Nov; 25 Suppl 1():S143-6. PubMed ID: 8577509
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Frontometaphyseal dysplasia.
    Holt JF; Thompson GR; Arenberg IK
    Radiol Clin North Am; 1972 Aug; 10(2):225-43. PubMed ID: 5044403
    [No Abstract]   [Full Text] [Related]  

  • 4. Shprintzen-Goldberg syndrome: case report.
    Topouzelis N; Markovitsi E; Antoniades K
    Cleft Palate Craniofac J; 2003 Jul; 40(4):433-6. PubMed ID: 12846610
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Rare Case Of Shprintzen-Goldberg Syndrome.
    Chitran P; Nair Sreela LS; Mathew P; Prasad TS
    J Ayub Med Coll Abbottabad; 2021; 33(1):155-158. PubMed ID: 33774974
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Short stature, mental retardation, craniosynostosis, Klippel-Feil syndrome, Scheuerman kyphosis, rib gaps and other distinctive skeletal and genital anomalies. A new syndrome?
    Kozlowski K; Sillence D; Taylor F
    Pediatr Radiol; 1993; 23(6):442-5. PubMed ID: 8255647
    [No Abstract]   [Full Text] [Related]  

  • 7. Frontometaphyseal dysplasia: neonatal radiographic diagnosis.
    Glass RB; Rosenbaum KN
    Am J Med Genet; 1995 May; 57(1):1-5. PubMed ID: 7645585
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Shprintzen-Goldberg syndrome. A case report.
    Seemanova E; Kozlowski K
    Radiol Med; 1997 Dec; 94(6):673-5. PubMed ID: 9524609
    [No Abstract]   [Full Text] [Related]  

  • 9. The radiology of Coffin-Lowry syndrome.
    Padley S; Hodgson SV; Sherwood T
    Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591
    [No Abstract]   [Full Text] [Related]  

  • 10. Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull.
    Saal HM; Bulas DI; Allen JF; Vezina LG; Walton D; Rosenbaum KN
    Am J Med Genet; 1995 Jul; 57(4):573-8. PubMed ID: 7573131
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Shprintzen-Goldberg syndrome: a rare disorder.
    Yadav S; Rawal G
    Pan Afr Med J; 2016; 23():227. PubMed ID: 27761171
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Frontometaphyseal dysplasia. A new syndrome.
    Gorlin RJ; Cohen MM
    Am J Dis Child; 1969 Sep; 118(3):487-94. PubMed ID: 5807657
    [No Abstract]   [Full Text] [Related]  

  • 13. Frontometaphyseal dysplasia: evidence for autosomal dominant inheritance.
    Kassner EG; Haller JO; Reddy VH; Mitarotundo A; Katz I
    AJR Am J Roentgenol; 1976 Dec; 127(6):927-33. PubMed ID: 998829
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Craniometaphyseal dysplasia--characteristic roentgen findings].
    Schröder C; Quirin A; Oppermann HC; Oldigs HD
    Klin Padiatr; 1992; 204(3):174-6. PubMed ID: 1614185
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Musculoskeletal manifestations of the Antley-Bixler syndrome.
    Rumball KM; Pang E; Letts RM
    J Pediatr Orthop B; 1999 Apr; 8(2):139-43. PubMed ID: 10218180
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo exon 1 missense mutations of SKI and Shprintzen-Goldberg syndrome: two new cases and a clinical review.
    Au PY; Racher HE; Graham JM; Kramer N; Lowry RB; Parboosingh JS; Innes AM;
    Am J Med Genet A; 2014 Mar; 164A(3):676-84. PubMed ID: 24357594
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Shprintzen-Goldberg syndrome: a clinical analysis.
    Greally MT; Carey JC; Milewicz DM; Hudgins L; Goldberg RB; Shprintzen RJ; Cousineau AJ; Smith WL; Judisch GF; Hanson JW
    Am J Med Genet; 1998 Mar; 76(3):202-12. PubMed ID: 9508238
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome.
    Adès LC; Morris LL; Power RG; Wilson M; Haan EA; Bateman JF; Milewicz DM; Sillence DO
    Am J Med Genet; 1995 Jul; 57(4):565-72. PubMed ID: 7573130
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The Antley-Bixler syndrome: two new cases.
    Hosalkar HS; Shah HS; Gujar PS; Shaw BA
    J Postgrad Med; 2001; 47(4):252-5. PubMed ID: 11832641
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Craniometadiaphyseal dysplasia, wormian bone type.
    Santolaya JM; Hall CM; García-Miñaur S; Delgado A
    Am J Med Genet; 1998 May; 77(3):241-5. PubMed ID: 9605592
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.