BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 3777025)

  • 1. Robin sequence and oligodactyly in mother and son.
    Robinow M; Johnson GF; Apesos J
    Am J Med Genet; 1986 Oct; 25(2):293-7. PubMed ID: 3777025
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Robin sequence and oligodactyly in mother and son--probably a further example of the postaxial acrofacial dysostosis syndrome.
    Meinecke P; Wiedemann HR
    Am J Med Genet; 1987 Aug; 27(4):953-7. PubMed ID: 3425604
    [No Abstract]   [Full Text] [Related]  

  • 3. Robin sequence with facial and digital anomalies in two half-brothers by the same mother.
    Chitayat D; Meunier CM; Hodgkinson KA; Azouz ME
    Am J Med Genet; 1991 Aug; 40(2):167-72. PubMed ID: 1897570
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Absence of fibula and ulna with oligodactyly, contractures, right-angle bowing of femora, abnormal facial morphology, cleft lip/palate and brain malformation in two sibs: a possibly new lethal syndrome.
    Pfeiffer RA; Stöss H; Voight HJ; Wündisch GF
    Am J Med Genet; 1988 Apr; 29(4):901-8. PubMed ID: 3400735
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The EEC syndrome. Report of six patients.
    Pashayan HM; Pruzansky S; Solomon L
    Birth Defects Orig Artic Ser; 1974; 10(7):105-27. PubMed ID: 4425508
    [No Abstract]   [Full Text] [Related]  

  • 6. Association of the Robin sequence with the fragile X syndrome.
    Lachiewicz AM; Hoegerman SF; Holmgren G; Holmberg E; Arinbjarnarson K
    Am J Med Genet; 1991 Dec; 41(3):275-8. PubMed ID: 1789278
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Aglossia-adactylia syndrome (special emphasis on the inheritance pattern).
    Tuncbilek E; Yalcin C; Atasu M
    Clin Genet; 1977 Jun; 11(6):421-3. PubMed ID: 880741
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation.
    Mathieu M; De Broca A; Bony H; Piussan C
    Genet Couns; 1993; 4(4):299-303. PubMed ID: 8110419
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial postaxial acrofacial dysostosis syndrome.
    Giannotti A; Digilio MC; Virgili Q; Obregon MG; Guadagni AM; Ventura T; Dallapiccola B
    J Med Genet; 1992 Oct; 29(10):752. PubMed ID: 1433242
    [No Abstract]   [Full Text] [Related]  

  • 10. The Gordon syndrome: autosomal dominant cleft palate, camptodactyly, and club feet.
    Robinow M; Johnson GF
    Am J Med Genet; 1981; 9(2):139-46. PubMed ID: 7258227
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ventricular extrasystoles with syncopal episodes, perodactyly, and Robin in sequence in three generations: a new inherited MCA syndrome?
    Stoll C; Kieny JR; Dott B; Alembik Y; Finck S
    Am J Med Genet; 1992 Feb; 42(4):480-6. PubMed ID: 1376967
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
    Guttmacher AE
    Am J Med Genet; 1993 Apr; 46(2):219-22. PubMed ID: 8484413
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial broad terminal phalanges with one individual showing additional anomalies.
    Pavone L; Sorge G; Pavone V; Rizzo R; Ruggieri M; Polizzi A; Opitz JM
    Am J Med Genet; 1997 Aug; 71(3):271-4. PubMed ID: 9268094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Stickler syndrome: report of four cases.
    Kulkarni ML; Sureshkumar C; George VG
    Ann Dent; 1993; 52(2):23-7. PubMed ID: 8267375
    [No Abstract]   [Full Text] [Related]  

  • 15. Acro-cardio-facial syndrome associated with neuroepithelial cyst: a case report.
    Sivasli O; Ozer EA; Ozer A; Aydinlioglu H; Helvaci M
    Genet Couns; 2007; 18(2):247-50. PubMed ID: 17710878
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Dysmaturity as symptom of the ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome].
    Porcelijn L; Maat-Kievit JA; van Haeringen A
    Tijdschr Kindergeneeskd; 1993 Jun; 61(3):96-9. PubMed ID: 8211943
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Marchesani syndrome.
    Amla I; Krishna GS; Mruthyunijaya GT
    J Indian Med Assoc; 1972 Dec; 59(12):517-20. PubMed ID: 4658301
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. [An unusual aglossia-adactylia syndrome (author's transl)].
    Deffez JP; Rostand B; Allain P; Brethaux J; Grimbert N; Van Cuc E
    Rev Stomatol Chir Maxillofac; 1981; 82(4):241-6. PubMed ID: 6944760
    [No Abstract]   [Full Text] [Related]  

  • 20. The Roberts syndrome.
    Freeman MV; Williams DW; Schimke RN; Temtamy SA; Vachier E; German J
    Birth Defects Orig Artic Ser; 1974; 10(5):87-95. PubMed ID: 4220010
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.