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 *

105 related articles for article (PubMed ID: 1659191)

  • 1. Oculodentodigital dysplasia syndrome associated with abnormal cerebral white matter.
    Gutmann DH; Zackai EH; McDonald-McGinn DM; Fischbeck KH; Kamholz J
    Am J Med Genet; 1991 Oct; 41(1):18-20. PubMed ID: 1659191
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oculodentodigital dysplasia with cerebral white matter abnormalities in a two-generation family.
    Norton KK; Carey JC; Gutmann DH
    Am J Med Genet; 1995 Jul; 57(3):458-61. PubMed ID: 7677152
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neurological manifestations of the oculodentodigital dysplasia syndrome.
    Loddenkemper T; Grote K; Evers S; Oelerich M; Stögbauer F
    J Neurol; 2002 May; 249(5):584-95. PubMed ID: 12021949
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Oculodentodigital dysplasia: study of ophthalmological and clinical manifestations in three boys with probably autosomal recessive inheritance.
    Frasson M; Calixto N; Cronemberger S; de Aguiar RA; Leão LL; de Aguiar MJ
    Ophthalmic Genet; 2004 Sep; 25(3):227-36. PubMed ID: 15512999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Central nervous system abnormalities in oculodentodigital dysplasia.
    Schrander-Stumpel CT; Franke CL
    Genet Couns; 1996; 7(3):233-5. PubMed ID: 8897047
    [No Abstract]   [Full Text] [Related]  

  • 6. Type III syndactyly and oculodentodigital dysplasia: a clinical spectrum.
    Schrander-Stumpel CT; De Groot-Wijnands JB; De Die-Smulders C; Fryns JP
    Genet Couns; 1993; 4(4):271-6. PubMed ID: 8110413
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Oculodentodigital dysplasia: ulnar-sided syndactyly and its associated disorders.
    Jones C; Baldrighi C; Mills J; Bush P; Ezaki M; Oishi S
    J Hand Surg Am; 2011 Nov; 36(11):1816-21. PubMed ID: 22036282
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for genetic anticipation in the oculodentodigital syndrome.
    Shapiro RE; Griffin JW; Stine OC
    Am J Med Genet; 1997 Jul; 71(1):36-41. PubMed ID: 9215766
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family.
    Amador C; Mathews AM; Del Carmen Montoya M; Laughridge ME; Everman DB; Holden KR
    J Child Neurol; 2008 Aug; 23(8):901-5. PubMed ID: 18660473
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Teaching neuroimages: oculodentodigital dysplasia: hypomyelination and syndactyly.
    Ganos C; Münchau A; Holst B; Schlüter G; Gerloff C; Uyanik G
    Neurology; 2012 Oct; 79(16):e140. PubMed ID: 23071171
    [No Abstract]   [Full Text] [Related]  

  • 11. A new GJA1 (connexin 43) mutation causing oculodentodigital dysplasia associated to uncommon features.
    de la Parra DR; Zenteno JC
    Ophthalmic Genet; 2007 Dec; 28(4):198-202. PubMed ID: 18161618
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complicated hereditary spastic paraparesis with cerebral white matter lesions.
    Gutmann DH; Fischbeck KH; Kamholz J
    Am J Med Genet; 1990 Jun; 36(2):251-7. PubMed ID: 2368815
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Progressive spastic paraplegia as a presentation of oculodentodigital syndrome].
    Nguyen K; Philip N; Suchet L; Azulay JP; Pouget J
    Rev Neurol (Paris); 2004 Jan; 160(1):83-5. PubMed ID: 14978398
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Neurological presentations of oculodentodigital dysplasia].
    Rudenskaya GE; Dyomina NA; Bliznetz EA; Khlebnikova OV; Dadaly EL; Polyakov AV
    Zh Nevrol Psikhiatr Im S S Korsakova; 2018; 118(5):85-91. PubMed ID: 29927410
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Brain anomalies in velo-cardio-facial syndrome.
    Mitnick RJ; Bello JA; Shprintzen RJ
    Am J Med Genet; 1994 Jun; 54(2):100-6. PubMed ID: 8074159
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the connexin 43 gene.
    van Es RJ; Wittebol-Post D; Beemer FA
    Int J Oral Maxillofac Surg; 2007 Sep; 36(9):858-60. PubMed ID: 17509830
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Delayed gastric emptying and chronic diarrhea in a patient with oculodentodigital dysplasia syndrome.
    Levine DS
    J Pediatr Gastroenterol Nutr; 1986; 5(2):329-33. PubMed ID: 3083083
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation in the GJA1 gene in a family with oculodentodigital dysplasia.
    Vasconcellos JP; Melo MB; Schimiti RB; Bressanim NC; Costa FF; Costa VP
    Arch Ophthalmol; 2005 Oct; 123(10):1422-6. PubMed ID: 16219735
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Oculodentodigital dysplasia: new ocular findings and a novel connexin 43 mutation.
    Gabriel LA; Sachdeva R; Marcotty A; Rockwood EJ; Traboulsi EI
    Arch Ophthalmol; 2011 Jun; 129(6):781-4. PubMed ID: 21670345
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.
    van der Knaap MS; Smit LM; Barth PG; Catsman-Berrevoets CE; Brouwer OF; Begeer JH; de Coo IF; Valk J
    Ann Neurol; 1997 Jul; 42(1):50-9. PubMed ID: 9225685
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.