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 *

96 related articles for article (PubMed ID: 3325020)

  • 21. [Ocular manifestations of trisomy 18].
    Ardouin M; Urvoy M; Lautridou A; Le Marec B; Senecal J
    Arch Ophtalmol Rev Gen Ophtalmol; 1972; 32(6):457-76. PubMed ID: 4264548
    [No Abstract]   [Full Text] [Related]  

  • 22. Pseudotrisomy 13 syndrome.
    Martínez-Frías ML; Urioste M; Martin M; Frías JL
    Am J Med Genet; 1992 Jun; 43(3):633-8. PubMed ID: 1605265
    [No Abstract]   [Full Text] [Related]  

  • 23. Trisomy 13 is associated with anorectal malformations.
    Lewis NA; Lander AD
    Arch Dis Child; 2007 Feb; 92(2):185. PubMed ID: 17264292
    [No Abstract]   [Full Text] [Related]  

  • 24. [Trisomy 13 syndrome, Patau syndrome].
    Tsukino R; Sasaki M
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):332-4. PubMed ID: 11057250
    [No Abstract]   [Full Text] [Related]  

  • 25. Holoprosencephaly, polydactyly and normal chromosomes: pseudo-trisomy 13?
    Hewitt BG; Seller MJ; Bennett CP; Maxwell DM
    Clin Genet; 1989 Aug; 36(2):141-3. PubMed ID: 2766571
    [No Abstract]   [Full Text] [Related]  

  • 26. [Medical genetic consultation in cyclopia].
    Kozlova SI; Korobova LI; Tsvetkova TG; Kulieva LM
    Akush Ginekol (Mosk); 1976 Dec; (12):45-51. PubMed ID: 1020777
    [No Abstract]   [Full Text] [Related]  

  • 27. Trisomy 13 syndrome and neural tube defects.
    Rodríguez JI; García M; Morales C; Morillo A; Delicado A
    Am J Med Genet; 1990 Aug; 36(4):513-6. PubMed ID: 2202219
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Trisomy 13 syndrome.
    Fukushima H; Harada T; Morita N; Paparella MM
    Otol Neurotol; 2008 Dec; 29(8):1209-10. PubMed ID: 18580543
    [No Abstract]   [Full Text] [Related]  

  • 29. Trisomy 4 in a fetus with cyclopia and other anomalies.
    Van Allen MI; Ritchie S; Toi A; Fong K; Winsor E
    Am J Med Genet; 1993 Apr; 46(2):193-7. PubMed ID: 8484409
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Prenatally detected congenital cystic adenomatoid malformation and postnatally diagnosed trisomy 13: case report and review of the literature.
    Turan O; Hirfanoğlu IM; Beken S; Biri A; Efetürk T; Atalay Y
    Turk J Pediatr; 2011; 53(3):337-41. PubMed ID: 21980820
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Duplication of 9q12-q33: a case report and implications for the dup(9q) syndrome.
    Stalker HJ; Aymé S; Delneste D; Scarpelli H; Vekemans M; Der Kaloustian VM
    Am J Med Genet; 1993 Feb; 45(4):456-9. PubMed ID: 8465850
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Pseudo-trisomy 13 syndrome.
    Cohen MM; Gorlin RJ
    Am J Med Genet; 1991 Jun; 39(3):332-5; discussion 336-7. PubMed ID: 1867286
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Two sibs with partial trisomy 2q.
    Barnicoat AJ; Abusaad I; Mackie CM; Robards MF
    Am J Med Genet; 1997 May; 70(2):166-70. PubMed ID: 9128937
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
    Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Pätau syndrome without trisomy karyotype? Danger of restricted thinking in syndrome diagnosis].
    Rode G; Duda V
    Z Geburtshilfe Perinatol; 1991; 195(3):143-5. PubMed ID: 1926974
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Partial trisomy 10q: further delineation of the clinical manifestations involving the segment 10q23-->10q24.
    Halpern GJ; Shohat M; Merlob P
    Ann Genet; 1996; 39(3):181-3. PubMed ID: 8839892
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Trisomy 13/trisomy 18 mosaicism in an infant.
    Abe K; Harada N; Itoh T; Hirakawa O; Niikawa N
    Clin Genet; 1996 Nov; 50(5):300-3. PubMed ID: 9007314
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Pediatric home care nursing of an infant with trisomy 13 (Patau syndrome)].
    Köck-Sauvagerd S
    Kinderkrankenschwester; 2001 Nov; 20(11):459-61. PubMed ID: 14584130
    [No Abstract]   [Full Text] [Related]  

  • 39. Congenital unilateral absence of orbit with anophthalmos and partial arhinia.
    Shorey P; Lobo G
    Indian J Ophthalmol; 1991; 39(3):132-3. PubMed ID: 1841889
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Further delineation of pseudotrisomy 13 syndrome: a case without polydactyly.
    Ramos-Arroyo MA; de Miguel C; Valiente A; Moreno-Laguna S
    Am J Med Genet; 1994 Apr; 50(2):177-9. PubMed ID: 8010349
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.