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 *

124 related articles for article (PubMed ID: 12784312)

  • 1. Mandibuloacral dysplasia with absent breast development.
    Cogulu O; Gunduz C; Arkun R; Darcan S; Kadioglu B; Ozkinay F; Ozkinay C
    Am J Med Genet A; 2003 Jun; 119A(3):391-2. PubMed ID: 12784312
    [No Abstract]   [Full Text] [Related]  

  • 2. Familial mandibuloacral dysplasia--a report of four cases.
    Prasad PV; Padmavathy L; Sethurajan S
    Int J Dermatol; 1998 Aug; 37(8):614-6. PubMed ID: 9732012
    [No Abstract]   [Full Text] [Related]  

  • 3. Long-term follow-up of cutaneous changes in siblings with mandibuloacral dysplasia who were originally considered to have hereditary sclerosing poikiloderma.
    Fryburg JS; Sidhu-Malik N
    J Am Acad Dermatol; 1995 Nov; 33(5 Pt 2):900-2. PubMed ID: 7593806
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Lethal neonatal mandibuloacral dysplasia.
    Seftel MD; Wright CA; Po PL; de Ravel TJ
    Am J Med Genet; 1996 Dec; 66(1):52-4. PubMed ID: 8957511
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mandibulo-acral dysplasia in a one-year-old boy.
    Vantrappen G; Feenstra L; Macours-Verelst C; Fryns JP
    Genet Couns; 2000; 11(1):49-52. PubMed ID: 10756428
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mandibulo-acral dysplasia.
    Hoeffel JC; Mainard L; Chastagner P; Hoeffel CC
    Skeletal Radiol; 2000 Nov; 29(11):668-71. PubMed ID: 11201039
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Severe insulin resistance and diabetes mellitus in mandibuloacral dysplasia.
    Freidenberg GR; Cutler DL; Jones MC; Hall B; Mier RJ; Culler F; Jones KL; Lozzio C; Kaufmann S
    Am J Dis Child; 1992 Jan; 146(1):93-9. PubMed ID: 1736653
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia.
    Agarwal AK; Fryns JP; Auchus RJ; Garg A
    Hum Mol Genet; 2003 Aug; 12(16):1995-2001. PubMed ID: 12913070
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mandibuloacral "dysplasia".
    Toriello HV
    Am J Med Genet; 1991 Oct; 41(1):138, 140. PubMed ID: 1951456
    [No Abstract]   [Full Text] [Related]  

  • 10. A novel homozygous LMNA mutation (p.Met540Ile) causes mandibuloacral dysplasia type A.
    Yassaee VR; Khojaste A; Hashemi-Gorji F; Ravesh Z; Toosi P
    Gene; 2016 Feb; 577(1):8-13. PubMed ID: 26602028
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mandibuloacral dysplasia: a rare progeroid syndrome. Two brothers confirm autosomal recessive inheritance.
    Pallotta R; Morgese G
    Clin Genet; 1984 Aug; 26(2):133-8. PubMed ID: 6467666
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Mandibuloacral dysplasia].
    Izumikawa Y
    Ryoikibetsu Shokogun Shirizu; 2001; (34 Pt 2):132. PubMed ID: 11528658
    [No Abstract]   [Full Text] [Related]  

  • 13. Another Italian family with mandibuloacral dysplasia: why does it seem more frequent in Italy?
    Tenconi R; Miotti F; Miotti A; Audino G; Ferro R; Clementi M
    Am J Med Genet; 1986 Jun; 24(2):357-64. PubMed ID: 3717214
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Syndromes and situations associated with congenital clavicular hypoplasia or agenesis.
    Hall BD
    Prog Clin Biol Res; 1982; 104():279-88. PubMed ID: 7163272
    [No Abstract]   [Full Text] [Related]  

  • 15. Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency.
    Agarwal AK; Zhou XJ; Hall RK; Nicholls K; Bankier A; Van Esch H; Fryns JP; Garg A
    J Investig Med; 2006 May; 54(4):208-13. PubMed ID: 17152860
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Failure of ossification of the occipital bone in mandibuloacral dysplasia type B.
    Haye D; Dridi H; Levy J; Lambert V; Lambert M; Agha M; Adjimi F; Kohlhase J; Lipsker D; Verloes A
    Am J Med Genet A; 2016 Oct; 170(10):2750-5. PubMed ID: 27410998
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gene expression profiling of fibroblasts from a human progeroid disease (mandibuloacral dysplasia, MAD #248370) through cDNA microarrays.
    Amati F; Biancolella M; D'Apice MR; Gambardella S; Mango R; Sbraccia P; D'Adamo M; Margiotti K; Nardone A; Lewis M; Novelli G
    Gene Expr; 2004; 12(1):39-47. PubMed ID: 15473259
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [A sterno-cleido-digital syndrome].
    Tscherninkov Z; Welitschkov S; Ditschev P
    Radiol Diagn (Berl); 1988; 29(2):257-60. PubMed ID: 2838867
    [No Abstract]   [Full Text] [Related]  

  • 19. Interrupted/bipartite clavicle as a diagnostic clue in Kabuki syndrome.
    Haanpää M; Schlecht H; Batra G; Clayton-Smith J; Douzgou S
    Am J Med Genet A; 2017 Apr; 173(4):1115-1118. PubMed ID: 28256057
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Bifid condyle of the mandible with associated polythelia and manual anomalies.
    Zohar Y; Laurian N
    J Laryngol Otol; 1987 Dec; 101(12):1315-9. PubMed ID: 3430056
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.