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 *

205 related articles for article (PubMed ID: 8487277)

  • 1. Otopalatodigital syndrome type II.
    Holder SE; Winter RM
    J Med Genet; 1993 Apr; 30(4):310-3. PubMed ID: 8487277
    [No Abstract]   [Full Text] [Related]  

  • 2. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P; Lefort G; Eglin MC; Rieu D; Sarda P
    Genet Couns; 1993; 4(4):289-94. PubMed ID: 8110417
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 Mar; 14(2):91-2. PubMed ID: 8469651
    [No Abstract]   [Full Text] [Related]  

  • 4. Oto-palato-digital syndrome, type II--an X-linked skeletal dysplasia.
    Brewster TG; Lachman RS; Kushner DC; Holmes LB; Isler RJ; Rimoin DL
    Am J Med Genet; 1985 Feb; 20(2):249-54. PubMed ID: 3976718
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Oto-palato-digital syndrome with features of type I and II in brothers.
    Horn D; Nitz I; Bollmann R
    Genet Couns; 1995; 6(3):233-40. PubMed ID: 8588852
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tricho-rhino-phalangeal syndrome.
    Kozlowski K; Blaim A; Malolepszy E
    Australas Radiol; 1972 Dec; 16(4):411-6. PubMed ID: 4661984
    [No Abstract]   [Full Text] [Related]  

  • 7. A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome).
    Merlob P; Grünebaum M; Reisner SH
    Acta Paediatr Scand; 1981 Mar; 70(2):275-7. PubMed ID: 6263040
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Oto-Palato-Digital syndrome in four generations of a large family.
    Pazzaglia UE; Beluffi G
    Clin Genet; 1986 Oct; 30(4):338-44. PubMed ID: 3791682
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The acrofacial dysostoses--a wide spectrum of overlapping phenotypes.
    Dimitrov B; Balikova I; Bradinova I; Zahariev D; Popova A; Simeonov E; De Smet L; Devriendt K; Fryns JP
    Genet Couns; 2005; 16(2):181-6. PubMed ID: 16080300
    [No Abstract]   [Full Text] [Related]  

  • 10. Oto-palato-digital syndrome type II.
    Stoll C; Alembik Y
    Genet Couns; 1994; 5(1):61-6. PubMed ID: 8031537
    [TBL] [Abstract][Full Text] [Related]  

  • 11. O--short stature with abnormalities of the cranium and limbs.
    Jorgenson RJ
    Birth Defects Orig Artic Ser; 1974; 10(5):249-51. PubMed ID: 4469995
    [No Abstract]   [Full Text] [Related]  

  • 12. The facio-digito-genital syndrome (Aarskog syndrome): a further delineation of the distinct radiological findings.
    Lizcano-Gil LA; Garcia-Cruz D; Cantu JM; Fryns JP
    Genet Couns; 1994; 5(4):387-92. PubMed ID: 7888143
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Craniofacial conodysplasia.
    Beals RK; Piatt JH; Zonana J
    J Pediatr Orthop; 1995; 15(5):633-6. PubMed ID: 7593576
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Refined mapping of the gene for otopalatodigital syndrome type I.
    Kosho T; Uemura T; Tanimura M; Ohashi H; Muroya K; Ogata T
    J Med Genet; 2002 Feb; 39(2):E7. PubMed ID: 11836376
    [No Abstract]   [Full Text] [Related]  

  • 15. The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia. Further evidence for autosomal recessive inheritance.
    Meinecke P; Fryns JP
    Clin Genet; 1985 Dec; 28(6):516-20. PubMed ID: 4075561
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Otopalatodigital syndrome type II associated with omphalocele: report of three cases.
    Young K; Barth CK; Moore C; Weaver DD
    Am J Med Genet; 1993 Feb; 45(4):481-7. PubMed ID: 8465856
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Hereditary type E brachydactylia. Apropos of a familial case].
    Gnamey D; Walbaum R; Fossati P; Prouvost JM
    Pediatrie; 1975 Mar; 30(2):153-9. PubMed ID: 165459
    [No Abstract]   [Full Text] [Related]  

  • 18. N--variable expressivity in craniocarpotarsal dysplasia.
    Wilson CD; Pearce WG
    Birth Defects Orig Artic Ser; 1974; 10(5):243-8. PubMed ID: 4220007
    [No Abstract]   [Full Text] [Related]  

  • 19. Otopalatodigital syndrome.
    Takato T; Fukuda O; Oda M
    Ann Plast Surg; 1985 Apr; 14(4):371-4. PubMed ID: 3994281
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Schinzel acrocallosal syndrome: a variant example of the Greig syndrome?
    Legius E; Fryns JP; Casaer P; Boel M; Eggermont E
    Ann Genet; 1985; 28(4):239-40. PubMed ID: 3879437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.