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 *

162 related articles for article (PubMed ID: 6589471)

  • 1. [Dento-maxillo-facial anomalies in the KBG syndrome].
    Tollaro I; v Bassarelli ; Calzolari C; Franchini F; Giovannucci Uzielli ML; Vieri PL
    Minerva Stomatol; 1984; 33(3):437-46. PubMed ID: 6589471
    [No Abstract]   [Full Text] [Related]  

  • 2. Six additional cases of the KBG syndrome: clinical reports and outline of the diagnostic criteria.
    Zollino M; Battaglia A; D'Avanzo MG; Della Bruna MM; Marini R; Scarano G; Cappa M; Neri G
    Am J Med Genet; 1994 Sep; 52(3):302-7. PubMed ID: 7810561
    [TBL] [Abstract][Full Text] [Related]  

  • 3. KBG syndrome: review of the literature and findings of 5 affected patients.
    Kumar H; Prabhu N; Cameron A
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep; 108(3):e72-9. PubMed ID: 19716495
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Maxillofacial and dental anomalies in multiple-abnormality syndromes. The clinical and therapeutic aspects in Sotos' syndrome].
    Staffolani N; Belcastro S; Guerra M
    Minerva Stomatol; 1994 Nov; 43(11):525-9. PubMed ID: 7739485
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Dento-maxillo-facial abnormalities and tricho-rhino-phalangeal syndrome: apropos of a case].
    Sommermater JI; Stoll C; Obry F; Bacon W; Haag R
    Rev Odontostomatol (Paris); 1978; 7(3):195-200. PubMed ID: 279071
    [No Abstract]   [Full Text] [Related]  

  • 6. The KBG syndrome-a syndrome of short stature, characteristic facies, mental retardation, macrodontia and skeletal anomalies.
    Herrmann J; Pallister PD; Tiddy W; Opitz JM
    Birth Defects Orig Artic Ser; 1975; 11(5):7-18. PubMed ID: 1218237
    [No Abstract]   [Full Text] [Related]  

  • 7. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F
    Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dento-skeletal implications of Klippel-Feil syndrome [a case report].
    Barbosa V; Maganzini AL; Nieberg LG
    N Y State Dent J; 2005 Jan; 71(1):48-51. PubMed ID: 15768912
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The KBG syndrome: an additional sporadic case.
    Mathieu M; Helou M; Morin G; Dolhem P; Devauchelle B; Piussan C
    Genet Couns; 2000; 11(1):33-5. PubMed ID: 10756425
    [TBL] [Abstract][Full Text] [Related]  

  • 10. KBG syndrome: clinical features and specific dental findings.
    Almandey AH; Anthonappa RP; King NM; Fung CW
    Pediatr Dent; 2010; 32(5):439-44. PubMed ID: 21070713
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Frontonasal dysplasia, macroblepharon, eyelid colobomas, ear anomalies, macrostomia, mental retardation, and CNS structural anomalies. A new syndrome?
    Guion-Almeida ML; Richieri-Costa A
    Clin Dysmorphol; 1999 Jan; 8(1):1-4. PubMed ID: 10327243
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Macrocephaly, facial abnormalities, disproportionate tall stature, and mental retardation--a sib observation.
    Bakker HD; Hennekam RC
    Am J Med Genet; 1997 Jun; 70(3):312-4. PubMed ID: 9188672
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Maxillofacial and dental abnormalities in some multiple abnormality syndromes. "Cri du chat" syndrome, Wilms' tumor-aniridia syndrome; Sotos syndrome; Goldenhar syndrome].
    Berio A; Trucchi R; Meliota M
    Minerva Pediatr; 1992 May; 44(5):223-9. PubMed ID: 1320183
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Coffin-Lowry syndrome in 2 brothers].
    Oguchi H; Oikawa K
    Shoni Shikagaku Zasshi; 1986; 24(1):191-9. PubMed ID: 3461521
    [No Abstract]   [Full Text] [Related]  

  • 15. Confirmation of Kapur-Toriello syndrome in an Italian patient.
    Zelante L; Candela MA; Savoia A; Gasparini P
    Clin Dysmorphol; 1999 Apr; 8(2):151-3. PubMed ID: 10319207
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital hypoplastic anaemia in a patient with a new multiple congenital anomalies-mental retardation syndrome.
    Mori PG; Priolo M; Lerone M; Pasino M; Caroli F; Cusano R; Seri M; Silengo MC
    Am J Med Genet; 1999 Nov; 87(1):36-9. PubMed ID: 10528244
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Kabuki Syndrome with additional dental findings: a case report.
    Cogulu D; Oncag O; Celen E; Ozkinay F
    J Dent Child (Chic); 2008; 75(2):185-7. PubMed ID: 18647516
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Kabuki syndrome, a congenital syndrome with multiple anomalies].
    den Biggelaar AM; Kuijpers-Jagtman AM; Bergé SJ; Katsaros C
    Ned Tijdschr Tandheelkd; 2006 Dec; 113(12):516-9. PubMed ID: 17193989
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Kabuki syndrome: a review.
    Adam MP; Hudgins L
    Clin Genet; 2005 Mar; 67(3):209-19. PubMed ID: 15691356
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Kabuki make-up syndrome. A report of 18 Spanish cases].
    Pascual-Castroviejo I; Pascual-Pascual SI; Velázquez-Fragua R; Palencia R
    Rev Neurol; 2005 Apr 16-30; 40(8):473-8. PubMed ID: 15861328
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.