BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 1656135)

  • 1. [Greig's cephalopolysyndactylia syndrome (McK 17570)].
    Lorenz P; Thiele H; Hinkel GK; Rupprecht E
    Kinderarztl Prax; 1991; 59(7-8):247-9. PubMed ID: 1656135
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. [Greig's syndrome. Neonatal radiologic manifestations].
    Merlob P; Grunebaum M; Mimouni F; Reisner SH
    J Radiol; 1984 Mar; 65(3):187-9. PubMed ID: 6325685
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. 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]  

  • 6. Syndrome identification case report 91: orofacial defects and polysyndactyly.
    Sugarman GI
    J Clin Dysmorphol; 1983; 1(1):16-9. PubMed ID: 6315899
    [No Abstract]   [Full Text] [Related]  

  • 7. Rubinstein-Taybi syndrome.
    Gellis SS; Feingold M
    Am J Dis Child; 1971 Apr; 121(4):327-8. PubMed ID: 5550739
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. Silver's syndrome with unusual presentations.
    Kapoor KL; Ahmad S; Karihalu PL; Ishar K
    J Indian Med Assoc; 1984 Nov; 82(11):408-10. PubMed ID: 6543559
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. A new form of spondyloperipheral dysplasia with facial dysmorphism, flattened vertebrae, hypoplastic pelvis, brachydactyly and soft tissue syndactyly.
    Kitoh H; Lachman RS
    Pediatr Radiol; 2001 Jan; 31(1):23-6. PubMed ID: 11200993
    [TBL] [Abstract][Full Text] [Related]  

  • 12. What syndrome is this? Disorganization syndrome.
    Hivnor CM; Yan AC; Aronson A; Crawford G; Seykora J; Honig PJ; Ming JE
    Pediatr Dermatol; 2007; 24(1):90-2. PubMed ID: 17300661
    [No Abstract]   [Full Text] [Related]  

  • 13. Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome?
    Filippi G
    Am J Med Genet; 1985 Dec; 22(4):821-4. PubMed ID: 4073130
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oto-palato-digital syndrome in an Iranian infant.
    Farhud DD; Walizadeh GR; Farhud I
    Monatsschr Kinderheilkd; 1989 Oct; 137(10):681-3. PubMed ID: 2555708
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Aglossia-adactylia. Apropos of a case. Review of the literature].
    Schuhl JF
    Ann Pediatr (Paris); 1986 Feb; 33(2):137-40. PubMed ID: 3008631
    [No Abstract]   [Full Text] [Related]  

  • 16. The Greig cephalopolysyndactyly syndrome in a Canadian family.
    Chudley AE; Houston CS
    Am J Med Genet; 1982 Nov; 13(3):269-76. PubMed ID: 6295159
    [No Abstract]   [Full Text] [Related]  

  • 17. Oculo-dento-digital dysplasia (OMIM *164200). Full manifestation of the syndrome in a 9.5 year-old girl and type III syndactyly in the father.
    Ioan DM; Dagomiz D; Fryns JP
    Genet Couns; 2002; 13(2):187-9. PubMed ID: 12150221
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The acrocallosal syndrome. Report of an additional case].
    Wendisch J; Lorenz P; Kabus M; Rupprecht E; Walther S
    Kinderarztl Prax; 1990 Jun; 58(6):315-21. PubMed ID: 2166860
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients.
    Chrzanowska KH; Fryns JP; Krajewska-Walasek M; Wisniewski L; Van den Berghe H
    Clin Genet; 1989 Feb; 35(2):157-60. PubMed ID: 2721025
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A pedigree of cervical stenosis, brachydactyly, syndactyly, and hyperopia.
    Iida H; Shikata J; Yamamuro T; Takeda N; Ueba Y
    Clin Orthop Relat Res; 1989 Oct; (247):80-6. PubMed ID: 2551554
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.