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 *

118 related articles for article (PubMed ID: 1057128)

  • 1. Oculodento-osseous dysplasia syndrome.
    Zach GA
    Oral Surg Oral Med Oral Pathol; 1975 Jul; 40(1):122-5. PubMed ID: 1057128
    [No Abstract]   [Full Text] [Related]  

  • 2. A family with oculodentodigital dysplasia.
    Weintraub DM; Baum JL; Pashayan HM
    Cleft Palate J; 1975 Jul; 12():323-9. PubMed ID: 1057461
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Oculodento-osseous dysplasia: heterogeneity or variable expression?
    Beighton P; Hamersma H; Raad M
    Clin Genet; 1979 Sep; 16(3):169-77. PubMed ID: 226298
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tricho-dento-osseous syndrome. Features of the hair and teeth.
    Wright JT; Roberts MW; Wilson AR; Kudhail R
    Oral Surg Oral Med Oral Pathol; 1994 May; 77(5):487-93. PubMed ID: 8028872
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dental management of oculodentodigital dysplasia: report of case.
    Dean JA; Jones JE; Vash BW
    ASDC J Dent Child; 1986; 53(2):131-4. PubMed ID: 2937820
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The syndrome of goldenhar affecting two siblings.
    Krause U
    Acta Ophthalmol (Copenh); 1970; 48(3):494-9. PubMed ID: 5536008
    [No Abstract]   [Full Text] [Related]  

  • 7. [An extensive form of mandibulo-facial dysostosis (Franceschetti) with malformations of the extremities and other congenital anomalies in a girl whose brother presents only an incomplete form of the syndrome (fistula auris congenita retrotragica)].
    Klein D; König H; Toller R
    Rev Otoneuroophtalmol; 1970 Nov; 42(7):432-40. PubMed ID: 5503545
    [No Abstract]   [Full Text] [Related]  

  • 8. Oculoauricular vertebral dysplasia. Its association with sensorineural deafness and other abnormalities.
    Budden SS; Robinson GC
    Am J Dis Child; 1973 Mar; 125(3):431-3. PubMed ID: 4692599
    [No Abstract]   [Full Text] [Related]  

  • 9. Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome.
    Jang MA; Kim EK; Now H; Nguyen NT; Kim WJ; Yoo JY; Lee J; Jeong YM; Kim CH; Kim OH; Sohn S; Nam SH; Hong Y; Lee YS; Chang SA; Jang SY; Kim JW; Lee MS; Lim SY; Sung KS; Park KT; Kim BJ; Lee JH; Kim DK; Kee C; Ki CS
    Am J Hum Genet; 2015 Feb; 96(2):266-74. PubMed ID: 25620203
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Intracranial calcification in oculodento-osseous dysplasia.
    Barnard A; Hamersma H; de Villiers JC; Beighton P
    S Afr Med J; 1981 May; 59(21):758-62. PubMed ID: 6262936
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Multiple synostosis].
    Czeizel E; Göblyös P
    Orv Hetil; 1993 Aug; 134(35):1917-20. PubMed ID: 8395675
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sotos syndrome with enamel hypoplasia: a case report.
    Inokuchi M; Nomura J; Mtsumura Y; Sekida M; Tagawa T
    J Clin Pediatr Dent; 2001; 25(4):313-6. PubMed ID: 11497013
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A genetic study and clinical classification of 154 cases of mandibulofacial dystosis (Franceschetti's syndrome), with descriptions of associated malformations].
    Vatré JL
    J Genet Hum; 1971 Mar; 19(1):17-100. PubMed ID: 5003458
    [No Abstract]   [Full Text] [Related]  

  • 14. Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second family.
    Wulfsberg EA; Campbell AB; Lurie IW; Eanet KR
    Am J Med Genet; 1996 Jun; 63(4):554-7. PubMed ID: 8826434
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The lacrimo-auriculo-dento-digital syndrome.
    Hollister DW; Klein SH; De Jager HJ; Lachman RS; Rimoin DL
    J Pediatr; 1973 Sep; 83(3):438-44. PubMed ID: 4725147
    [No Abstract]   [Full Text] [Related]  

  • 16. Mandibulofacial dysostosis with ectopia lentis.
    Kirkham TH
    Am J Ophthalmol; 1970 Dec; 70(6):947-9. PubMed ID: 5490623
    [No Abstract]   [Full Text] [Related]  

  • 17. Goldenhar's syndrome: two cases of oculo-auriculo-vertebral dysplasia occurring in full-blood Australian Aboriginal sisters.
    Kirke DK
    Aust Paediatr J; 1970 Mar; 6(1):213-4. PubMed ID: 5520428
    [No Abstract]   [Full Text] [Related]  

  • 18. Goldenhar's syndrome: two cases of oculo-auriculo-vertebral dysplasia occurring in full-blood Australian aboriginal sisters.
    Kirke DK
    Aust Paediatr J; 1970 Dec; 6(4):213-4. PubMed ID: 5527614
    [No Abstract]   [Full Text] [Related]  

  • 19. [Inguinal hernia, hydrocele, umbilical cyst and osseous manifestations in Berry-Treacher Collins syndrome (mandibulofacial dysostosis-FranceschettZwahlen-Klein syndrome). Case report and review of the literature].
    Saidi M; Chagnon J
    Union Med Can; 1970 May; 99(5):882-90. PubMed ID: 5450383
    [No Abstract]   [Full Text] [Related]  

  • 20. [Oculo-dento-digital dysplasia. (Observations in mother and child)].
    Pfeiffer RA; Erpenstein H; Jünemann G
    Klin Monbl Augenheilkd; 1968; 152(2):247-62. PubMed ID: 4970609
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.