BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 4102717)

  • 1. Clinical picture of two newborns with trisomy D.
    Jaworska M; Majlert T; Stolarska A
    Acta Chir Plast; 1971; 13(1):1-6. PubMed ID: 4102717
    [No Abstract]   [Full Text] [Related]  

  • 2. Trisomy E with multiple congenital anomalies.
    Biswas B; Heycock JB
    Br J Clin Pract; 1973 Jul; 27(7):269-70. PubMed ID: 4727309
    [No Abstract]   [Full Text] [Related]  

  • 3. [Trisomy due to transmitted translocation t(13 q , 14 q ). Estimation of recurrence risks].
    Belaisch G; Despres P; Plainfosse B; Rethore O; Emerit I; Loewe-Lyon S; Lejeune J; Seringe P
    Arch Fr Pediatr; 1971 Oct; 28(8):865-74. PubMed ID: 5123542
    [No Abstract]   [Full Text] [Related]  

  • 4. [Trisomy 13: a clinical study].
    Saraux H; Chigot PL
    J Genet Hum; 1966; 15():Suppl:293-302. PubMed ID: 5996513
    [No Abstract]   [Full Text] [Related]  

  • 5. [Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation].
    Stoll C; Halb A
    Pediatrie; 1974; 29(7):725-9. PubMed ID: 4456285
    [No Abstract]   [Full Text] [Related]  

  • 6. Are 1q plus chromosomes harmless?
    Gardner RJ; McCreanor HR; Parslow MI; Veale AM
    Clin Genet; 1974; 6(5):383-93. PubMed ID: 4434654
    [No Abstract]   [Full Text] [Related]  

  • 7. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Butler LJ; Eades SM; France NE
    Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708
    [No Abstract]   [Full Text] [Related]  

  • 8. Familial D-D translocation. A family showing transmission through three generations; a case with multiple congenital malformations, and a case of regular 21-trisomic Down's syndrome.
    Visfeldt J
    Acta Pathol Microbiol Scand; 1969; 75(4):545-54. PubMed ID: 4246134
    [No Abstract]   [Full Text] [Related]  

  • 9. [Trisomy syndrome D (47, XY, D+) in a newborn].
    Majlert T; Jaworska M; Stolarska A
    Pediatr Pol; 1970 Nov; 45(11):1379-82. PubMed ID: 5496174
    [No Abstract]   [Full Text] [Related]  

  • 10. Osseous malformations associated with chromosome abnormalities.
    Weiss L; Reynolds WA
    Orthop Clin North Am; 1972 Nov; 3(3):713-32. PubMed ID: 4264453
    [No Abstract]   [Full Text] [Related]  

  • 11. Autosomal chromosome aberrations in ophthalmology.
    Francois J
    Int Ophthalmol Clin; 1968; 8(4):839-910. PubMed ID: 4244691
    [No Abstract]   [Full Text] [Related]  

  • 12. [A case of cyclopia with 13-15 trisomy].
    Bugnon C; Gainet F; Royer J; Maire P
    Ann Ocul (Paris); 1972 Nov; 205(11):1181-94. PubMed ID: 4196609
    [No Abstract]   [Full Text] [Related]  

  • 13. [D trisomy. 2 cases with characteristic phenotype].
    Giovannucci ML; Calabri G; Paoli A
    Riv Clin Pediatr; 1969; 82():320-9. PubMed ID: 5405486
    [No Abstract]   [Full Text] [Related]  

  • 14. [Trisomy 18 in 2 newborn infants with rare abnormalities in one of them].
    Bruni L; Castello MA; Crucioli V; Zucco V
    Riv Ostet Ginecol; 1969 Feb; 24(2):60-73. PubMed ID: 5399531
    [No Abstract]   [Full Text] [Related]  

  • 15. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S; Jinorose U
    Am J Med Genet; 1994 Jan; 49(2):207-10. PubMed ID: 8116670
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Clinical manifestations in 2 cases of trisomy E].
    Białecki M; Słuzewska H
    Pediatr Pol; 1975 Feb; 50(2):229-33. PubMed ID: 1114039
    [No Abstract]   [Full Text] [Related]  

  • 17. II. A review of clinical syndromes associated with aberrations of the autosomes.
    Williams JD; Summitt RL
    J Tenn Med Assoc; 1971 Apr; 64(4):310-7. PubMed ID: 4252589
    [No Abstract]   [Full Text] [Related]  

  • 18. [Clinical diagnosis of Patau's syndrome].
    Laziuk GI; Kravtsova GI; Savenko LA; Usova IuI; Usoev SS
    Vopr Okhr Materin Det; 1973 Jun; 18(6):83-8. PubMed ID: 4744196
    [No Abstract]   [Full Text] [Related]  

  • 19. Distal trisomy 14q due to tandem duplication (q24 leads to q32).
    Orye E; Van Bever H; Desimpel H
    Ann Genet; 1983; 26(4):238-9. PubMed ID: 6607705
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Trisomy 18: Edward's syndrome (a case report of 3 cases).
    Bharucha BA; Agarwal UM; Savliwala AS; Kolluri R; Kumta NB
    J Postgrad Med; 1983 Apr; 29(2):129-32. PubMed ID: 6631764
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.