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 *

127 related articles for article (PubMed ID: 15365460)

  • 1. Catel-Manzke syndrome: a case report of a female with severely malformed hands and feet. An extension of the phenotype or a new syndrome?
    Clarkson JHW; Homfray T; Heron CW; Moss AL
    Clin Dysmorphol; 2004 Oct; 13(4):237-240. PubMed ID: 15365460
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Catel-Manzke syndrome without cleft palate: a case report.
    Puri RD; Phadke SR
    Clin Dysmorphol; 2003 Oct; 12(4):279-81. PubMed ID: 14564220
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel-Manzke syndrome in a fetus.
    Schoner K; Bald R; Horn D; Rehder H; Kornak U; Ehmke N
    Am J Med Genet A; 2017 Jun; 173(6):1694-1697. PubMed ID: 28422407
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Catel-Manzke syndrome without Manzke dysostosis.
    Miller DE; Chow P; Gallagher ER; Perkins JA; Wenger TL
    Am J Med Genet A; 2020 Mar; 182(3):437-440. PubMed ID: 31833187
    [TBL] [Abstract][Full Text] [Related]  

  • 5. TGDS pathogenic variants cause Catel-Manzke syndrome without hyperphalangy.
    Boschann F; Stuurman KE; de Bruin C; van Slegtenhorst M; van Duyvenvoorde HA; Kant SG; Ehmke N
    Am J Med Genet A; 2020 Mar; 182(3):431-436. PubMed ID: 31769200
    [TBL] [Abstract][Full Text] [Related]  

  • 6. IMPAD1 mutations in two Catel-Manzke like patients.
    Nizon M; Alanay Y; Tuysuz B; Kiper PO; Geneviève D; Sillence D; Huber C; Munnich A; Cormier-Daire V
    Am J Med Genet A; 2012 Sep; 158A(9):2183-7. PubMed ID: 22887726
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A patient with hyperphalangism: the milder phenotype of Catel-Manzke syndrome.
    Kiraz A; Tubas F; Ekinci Y; Dögen ME; Varli M
    Clin Dysmorphol; 2013 Oct; 22(4):169-171. PubMed ID: 24326962
    [No Abstract]   [Full Text] [Related]  

  • 8. Catel-Manzke digitopalatal syndrome or Temtamy preaxial brachydactyly hyperphalangism syndrome?
    Temtamy SA
    Clin Dysmorphol; 2005 Oct; 14(4):211. PubMed ID: 16155426
    [No Abstract]   [Full Text] [Related]  

  • 9. Unusual combination of limb malformations in the same patient: brachydactyly with syndactyly and postaxial polydactyly of the hands and postaxial oligodactyly of the feet.
    Ferda Percin E; Yilmaz S
    Clin Dysmorphol; 2003 Oct; 12(4):283-4. PubMed ID: 14564221
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Congenital radioulnar synostosis presenting in adulthood - a case report.
    Alsharif MHK; Almasaad JM; Taha KM; Elamin AY; Bakhit NM; Noureddin MA; Mahdi AAA
    Pan Afr Med J; 2020; 36():75. PubMed ID: 32774634
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A mother and daughter with a novel phenotype of hand and foot abnormalities and severe pectus excavatum.
    Low K; Smith J; Lee S; Newbury-Ecob R
    Am J Med Genet A; 2013 Aug; 161A(8):2056-9. PubMed ID: 23824731
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An unusual case of preaxial polydactyly of the hands and feet: a case report.
    Al-Qattan MM; Hashem FK; Al Malaq A
    J Hand Surg Am; 2002 May; 27(3):498-502. PubMed ID: 12015726
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Catel-Manzke syndrome: two new patients and a critical review of the literature.
    Manzke H; Lehmann K; Klopocki E; Caliebe A
    Eur J Med Genet; 2008; 51(5):452-65. PubMed ID: 18501694
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Skeletal abnormalities of hands and feet in Laurence-Moon-Bardet-Biedl (LMBB) syndrome: a radiographic study.
    Rudling O; Riise R; Tornqvist K; Jonsson K
    Skeletal Radiol; 1996 Oct; 25(7):655-60. PubMed ID: 8915050
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hand-foot-genital syndrome: the importance of hallux varus.
    Cleveland RH; Holmes LB
    Pediatr Radiol; 1990; 20(5):339-43. PubMed ID: 2349017
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Symbrachydactyly involving both the hand and foot. A report of two cases.
    Uchida T; Kojima T; Hirakawa M; Uchida M
    Handchir Mikrochir Plast Chir; 1995 Jan; 27(1):51-4. PubMed ID: 7705729
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hands and feet in the Apert syndrome.
    Cohen MM; Kreiborg S
    Am J Med Genet; 1995 May; 57(1):82-96. PubMed ID: 7645606
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Facial dysmorphism, multiple pigmented nevi, osteoporosis, brachydactyly, and other skeletal changes in a male: a new syndrome?
    Oktenli C; Ulucan H; Sağlam M; Gül D
    Clin Dysmorphol; 2003 Apr; 12(2):149-51. PubMed ID: 12868484
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Short stature, unusual face, delta phalanx, and abnormal vertebrae and ribs in a girl born to half-siblings.
    Pogue R; Marques FA; Kopacek C; Rosa RCM; Dorfman LE; Mazzeu JF; Flores JAM; Zen PRG; Rosa RFM
    Am J Med Genet A; 2017 May; 173(5):1152-1158. PubMed ID: 28371255
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Vertebral anomalies in a new family with ODED syndrome.
    Piersall LD; Dowton SB; McAlister WH; Waggoner DJ
    Clin Genet; 2000 Jun; 57(6):444-8. PubMed ID: 10905665
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.