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 *

156 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 8.