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 *

129 related articles for article (PubMed ID: 1071345)

  • 1. [Genetic aspects of craniofacial dysostoses: the Crouzon disease and the d'Apert-Crouzon disease].
    Lemaitre A; Van Reck J
    Acta Stomatol Belg; 1976; 73(3):279-85. PubMed ID: 1071345
    [No Abstract]   [Full Text] [Related]  

  • 2. Apert syndrome variant with overlapping features of Crouzon syndrome.
    Mukundan C; Radha TR; Rajakumari TK; Kapilamoorthy TR; Sharma RN
    J Assoc Physicians India; 2000 Aug; 48(8):842-4. PubMed ID: 11273485
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Acrocephalosyndactylia--Vogt syndrome].
    Fehlow P; Walther F
    Psychiatr Neurol Med Psychol (Leipz); 1985 Jun; 37(6):323-9. PubMed ID: 4034800
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [The problem of diagnosis and risk in cases of acrocephaly].
    Predescu V; Christodorescu D
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1975; 20(3):229-36. PubMed ID: 1085470
    [No Abstract]   [Full Text] [Related]  

  • 5. [Case of Aperts'-Crouzon syndrome in a 6-year old boy].
    Pawłowska M; Czerwionka-Szaflarska M; Swincow G; Nowicka C
    Przegl Lek; 1994; 51(7):315-8. PubMed ID: 7871207
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Greig's syndrome of hypertelorism].
    Pendl G; Zimprich H
    Helv Paediatr Acta; 1971 Aug; 26(3):319-25. PubMed ID: 5116166
    [No Abstract]   [Full Text] [Related]  

  • 7. [Crouzon syndrome (Mc K 12350)].
    Mitulla B; Hinkel GK; Lorenz P
    Kinderarztl Prax; 1991 Sep; 59(9):278-80. PubMed ID: 1942786
    [No Abstract]   [Full Text] [Related]  

  • 8. Apert's syndrome. Report of two cases in the Bantu.
    Schorn D; Vorster BJ; van Rooyen RJ
    S Afr Med J; 1972 Jan; 46(2):32-5. PubMed ID: 5058499
    [No Abstract]   [Full Text] [Related]  

  • 9. [Crouzon-Apert syndrome (dysostosis craniodigito-facialis)].
    WIETESKA H
    Pol Przegl Radiol Med Nukl; 1961; 25():47-58. PubMed ID: 13785160
    [No Abstract]   [Full Text] [Related]  

  • 10. [The Apert syndrome. Cytogenetic observations].
    Gualandri V; Milesi M; Turuani E
    Minerva Chir; 1966 Jul; 21(13):614-8. PubMed ID: 5968404
    [No Abstract]   [Full Text] [Related]  

  • 11. [Crouzon syndrome].
    Murano I
    Nihon Rinsho; 2006 Sep; Suppl 3():416-7. PubMed ID: 17022577
    [No Abstract]   [Full Text] [Related]  

  • 12. [A case of Crouzon's syndrome with coexistance of other congenital anomalies (author's transl)].
    Kowalski M; Paszkowska M; Bryjanowska L
    Klin Oczna; 1977 Oct; 47(10):445-7. PubMed ID: 926659
    [No Abstract]   [Full Text] [Related]  

  • 13. Recent advances in craniofacial genetics.
    Scheuerle AE
    J Craniofac Surg; 1995 Nov; 6(6):440-2. PubMed ID: 9020731
    [No Abstract]   [Full Text] [Related]  

  • 14. Crouzons syndrome: a case report.
    Arathi R; Sagtani A; Baliga M
    J Indian Soc Pedod Prev Dent; 2007; 25 Suppl():S10-2. PubMed ID: 17921633
    [TBL] [Abstract][Full Text] [Related]  

  • 15. On the nosology of severe acrofacial dysostosis with limb deficiency.
    Fryns JP
    Am J Med Genet; 1999 Jan; 82(3):282-3. PubMed ID: 10215555
    [No Abstract]   [Full Text] [Related]  

  • 16. [Hereditary craniofacial dysostosis (Morbus Crouzon)].
    Ludányi I; Bottlik G; Frey J
    Orv Hetil; 1969 Aug; 110(34):1979-82. PubMed ID: 5388551
    [No Abstract]   [Full Text] [Related]  

  • 17. Comparative study of normal, Crouzon, and Apert craniofacial morphology using finite element scaling analysis.
    Richtsmeier JT
    Am J Phys Anthropol; 1987 Dec; 74(4):473-93. PubMed ID: 3442299
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dentofacial characteristics in Apert syndrome: a case report.
    Batra P; Duggal R; Parkash H
    J Indian Soc Pedod Prev Dent; 2002 Sep; 20(3):118-23. PubMed ID: 12435011
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.
    Preston RA; Post JC; Keats BJ; Aston CE; Ferrell RE; Priest J; Nouri N; Losken HW; Morris CA; Hurtt MR
    Nat Genet; 1994 Jun; 7(2):149-53. PubMed ID: 7920632
    [TBL] [Abstract][Full Text] [Related]  

  • 20. On the classification of the acrocephalosyndactyly syndromes.
    Escobar V; Bixler D
    Clin Genet; 1977 Sep; 12(3):169-78. PubMed ID: 908170
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.