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 *

190 related articles for article (PubMed ID: 5006137)

  • 1. Mesoectodermal dysplasia of the iris and cornea, mental retardation and myopathy: a sporadic case.
    Summitt RL; Hiatt RL; Duenas D; Johnson WW
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):129-35. PubMed ID: 5006137
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Variability of clinical manifestations in the family with Axenfeld-Rieger syndrome].
    Kamińska A; Sokołowska-Oracz A; Pawluczyk-Dyjecińska M; Szaflik JP
    Klin Oczna; 2007; 109(7-9):321-6. PubMed ID: 18260289
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SHORT syndrome: a case with high hyperopia and astigmatism.
    Bonnel S; Dureau P; LeMerrer M; Dufier JL
    Ophthalmic Genet; 2000 Dec; 21(4):235-8. PubMed ID: 11135494
    [TBL] [Abstract][Full Text] [Related]  

  • 4. New autosomal recessive multiple congenital abnormalities/mental retardation syndrome with craniofacial dysmorphism absent corpus callosum, iris colobomas and connective tissue dysplasia.
    Temtamy SA; Salam MA; Aboul-Ezz EH; Hussein HA; Helmy SA; Shalash BA
    Clin Dysmorphol; 1996 Jul; 5(3):231-40. PubMed ID: 8818452
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [New hereditary syndrome with mental retardation].
    Marincheva GS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990; 90(3):66-9. PubMed ID: 2163174
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Craniotubular dysplasia with severe postnatal growth retardation, mental retardation, ectodermal dysplasia, and loose skin: Lenz-Majewski-like syndrome.
    Nishimura G; Harigaya A; Kuwashima M; Kuwashima S
    Am J Med Genet; 1997 Jul; 71(1):87-92. PubMed ID: 9215775
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Townes-Brocks syndrome.
    Powell CM; Michaelis RC
    J Med Genet; 1999 Feb; 36(2):89-93. PubMed ID: 10051003
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable types.
    Verloes A; Journel H; Elmer C; Misson JP; Le Merrer M; Kaplan J; Van Maldergem L; Deconinck H; Meire F
    Am J Med Genet; 1993 Apr; 46(2):132-7. PubMed ID: 8484397
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Bilateral prominent schwalbe ring in the anterior chamber in a patient with axenfeld-rieger syndrome and megalocornea.
    Espana EM; Mora R; Liebmann J; Ritch R
    Cornea; 2007 Apr; 26(3):379-81. PubMed ID: 17413972
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Joubert's syndrome: report of 12 cases].
    Barreirinho MS; Teixeira J; Moreira NC; Bastos S; Gonçalvez S; Barbot MC
    Rev Neurol; 2001 May 1-15; 32(9):812-7. PubMed ID: 11424029
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Dental anomalies, speech defects and orofacial muscle function disorders (III)].
    Burckhardt R; Schleicher A
    Quintessenz; 1982 Nov; 33(11):2261-8. PubMed ID: 6963447
    [No Abstract]   [Full Text] [Related]  

  • 12. [Dental anomalies, speech defects and orofacial muscle function disorders (II)].
    Burckhardt R; Schleicher A
    Quintessenz; 1982 Oct; 33(10):2029-34. PubMed ID: 6963440
    [No Abstract]   [Full Text] [Related]  

  • 13. Rieger's syndrome: (oligodontia and primary mesodermal dysgenesis of the iris) clinical features and report of an isolated case.
    Wesley RK; Baker JD; Golnick AL
    J Pediatr Ophthalmol Strabismus; 1978; 15(2):67-70. PubMed ID: 105118
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Megalocornea-mental retardation syndrome.
    Mukherjee SB; Juneja M
    Indian Pediatr; 2005 Aug; 42(8):835-6. PubMed ID: 16141491
    [No Abstract]   [Full Text] [Related]  

  • 15. Megalocornea-mental retardation syndrome: an additional case.
    Antiñolo G; Rufo M; Borrego S; Morales C
    Am J Med Genet; 1994 Aug; 52(2):196-7. PubMed ID: 7802008
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mental retardation, short stature, almond-shaped eyes, small downturned mouth and coned epiphyses: a new case of Hunter-Fraser syndrome.
    Van Maldergem L; Gillerot Y; Perlmutter N; Wetzburger C; Koulischer L
    Am J Med Genet; 1990 Oct; 37(2):283-5. PubMed ID: 2248298
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Dyngenesis mesodermalis corneae et iridis. Rieger's syndrome].
    Tĕsínský P; Vydrová J
    Cesk Oftalmol; 1979 Sep; 35(5):367-73. PubMed ID: 535065
    [No Abstract]   [Full Text] [Related]  

  • 18. The Rieger syndrome: orofacial manifestations. Case report of a rare condition.
    Singh J; Pannu K; Lehl G
    Quintessence Int; 2003 Oct; 34(9):689-92. PubMed ID: 14982223
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A syndrome with juvenile cataract, cerebellar atrophy, mental retardation and myopathy.
    Herva R; von Wendt L; von Wendt G; Saukkonen AL; Leisti J; Dubowitz V
    Neuropediatrics; 1987 Aug; 18(3):164-9. PubMed ID: 3683758
    [TBL] [Abstract][Full Text] [Related]  

  • 20. "New" ectodermal dysplasia with mental retardation and syndactyly.
    Ilyina HG; Amoashy DS; Grygory HA
    Am J Med Genet; 1995 Sep; 58(4):345-7. PubMed ID: 8533843
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.