BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 5455786)

  • 1. Coexisting familial abnormalities of karyotype and phenotype. Chromosome 16 and an unusual form of cutis laxa with skin webs.
    Garson OM; Baikie AG; O'Brien BM
    Med J Aust; 1970 Aug; 2(5):235-8. PubMed ID: 5455786
    [No Abstract]   [Full Text] [Related]  

  • 2. [Generalized Marfanoid congenital cutis laxa with lethal outcome: type V].
    Larrègue M; Bonneau D; Boureau C; De Giacomoni P
    Ann Dermatol Venereol; 1990; 117(11):823-4. PubMed ID: 2099692
    [No Abstract]   [Full Text] [Related]  

  • 3. [Congenital generalized cutis laxa: 5 cases].
    Rybojad M; Baumann C; Godeau G; Moraillon I; Prigent F; Morel P; Bourrat E
    Ann Dermatol Venereol; 1999 Apr; 126(4):317-9. PubMed ID: 10421933
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Male with type II autosomal recessive cutis laxa.
    Imaizumi K; Kurosawa K; Makita Y; Masuno M; Kuroki Y
    Clin Genet; 1994 Jan; 45(1):40-3. PubMed ID: 8149651
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple congenital skin webbing with cutis laxa.
    O'Brien BM; Garson OM; Baikie AG; Dooley BJ
    Br J Plast Surg; 1970 Oct; 23(4):329-36. PubMed ID: 4394470
    [No Abstract]   [Full Text] [Related]  

  • 6. Further delineation of 7p trisomy. Case report and review of literature.
    Pallotta R; Dalprà L; Fusilli P; Zuffardi O
    Ann Genet; 1996; 39(3):152-8. PubMed ID: 8839888
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Phenotype and karyotype interrelationships in chromosomal diseases].
    Prokof'eva-Bel'govska ; Grinberg KN; Revazov AA; Mikel'saar AV; Kuliev AM
    Vestn Akad Med Nauk SSSR; 1973; 28(1):37-44. PubMed ID: 4797784
    [No Abstract]   [Full Text] [Related]  

  • 8. Duplication and deletion 11q23-q24 recombinants in two offspring of an intrachromosomal insertion ("shift") carrier.
    Forsythe MG; Walker H; Weiss L; Roberson JR; Worsham MJ; Babu VR; Van Dyke DL
    Henry Ford Hosp Med J; 1988; 36(4):183-6. PubMed ID: 3250948
    [No Abstract]   [Full Text] [Related]  

  • 9. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
    Morava E; Lefeber DJ; Urban Z; de Meirleir L; Meinecke P; Gillessen Kaesbach G; Sykut-Cegielska J; Adamowicz M; Salafsky I; Ranells J; Lemyre E; van Reeuwijk J; Brunner HG; Wevers RA
    Eur J Hum Genet; 2008 Jan; 16(1):28-35. PubMed ID: 17971833
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial 18 q- syndrome.
    Law EM; Masterson JG
    Ann Genet; 1969 Dec; 12(4):215-22. PubMed ID: 5309411
    [No Abstract]   [Full Text] [Related]  

  • 11. Trisomy 18 associated with a familial translocation t(Bq-; 18q+).
    France NE; Butler LJ
    Ann Genet; 1969 Mar; 12(1):46-50. PubMed ID: 5306711
    [No Abstract]   [Full Text] [Related]  

  • 12. A case of 18q- in a t(18q-;6p+) family.
    Jacobsen P; Mikkelsen M; Niebuhr E; de Grouchy J
    Ann Genet; 1971 Mar; 14(1):41-8. PubMed ID: 5314293
    [No Abstract]   [Full Text] [Related]  

  • 13. Sotos syndrome and cutis laxa.
    Robertson SP; Bankier A
    J Med Genet; 1999 Jan; 36(1):51-6. PubMed ID: 9950366
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Familial occurence of abnormal karyotype 14p+].
    Balícek P; Zizka J
    Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove Suppl; 1975; 19(1):155-9. PubMed ID: 1071482
    [No Abstract]   [Full Text] [Related]  

  • 15. Cutis laxa type II and wrinkly skin syndrome: distinct phenotypes.
    Gupta N; Phadke SR
    Pediatr Dermatol; 2006; 23(3):225-30. PubMed ID: 16780467
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Brief clinical report: the dup(17p) syndrome.
    Feldman GM; Baumer JG; Sparkes RS
    Am J Med Genet; 1982 Mar; 11(3):299-304. PubMed ID: 7081295
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Anomaly of chromosomic structure (46,XX,17q+) in a polymalformed child].
    Walbaum R; Dupuis C; Dehaene P; Delmas-Marsalet Y
    Ann Genet; 1968 Mar; 11(1):53-5. PubMed ID: 5301757
    [No Abstract]   [Full Text] [Related]  

  • 18. Partial deletion of long arms of chromosome 18.
    Kushnick T; Matsushita G
    Pediatrics; 1968 Jul; 42(1):194-7. PubMed ID: 5657675
    [No Abstract]   [Full Text] [Related]  

  • 19. Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms.
    Eriksson B; Fraccaro M; Hultén M; Lindsten J; Thorén C; Tiepolo L
    Ann Genet; 1971 Dec; 14(4):281-90. PubMed ID: 5316133
    [No Abstract]   [Full Text] [Related]  

  • 20. [A patient with ring chromosome 13].
    Hammond A; Bijlsma JB
    Ned Tijdschr Geneeskd; 1981 May; 125(19):752-5. PubMed ID: 7242723
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.