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 *

76 related articles for article (PubMed ID: 3866853)

  • 1. Partial 15q trisomy: report of three siblings.
    Boraz RA; Schimke RN; Collins D
    J Pedod; 1985; 10(1):89-96. PubMed ID: 3866853
    [No Abstract]   [Full Text] [Related]  

  • 2. Partial 2p trisomy (p21 leads to pter) in two siblings of a family with a 2p-:15q+ translocation.
    Armendares S; Salamanca-Gómez F
    Clin Genet; 1978 Jan; 13(1):17-24. PubMed ID: 624187
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cleft palate and multiple anomalies in one of two siblings with partial 13 trisomy.
    Kaye CI; Booth CW; Meeker D; Nadler HL
    Cleft Palate J; 1977 Jul; 14(3):244-8. PubMed ID: 267527
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Distal trisomy 15q].
    Turleau C; de Grouchy J; Chavin-Colin F; Roubin M
    Ann Genet; 1977 Sep; 20(3):214-6. PubMed ID: 304707
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial trisomy 16q resulting from maternal translocation 11p/16q.
    Calva P; Frias S; Carnevale A; Reyes P
    Ann Genet; 1984; 27(2):122-5. PubMed ID: 6331790
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A case of partial trisomy 13 with robertsonian translocation on chromosome 15 in a 3-year-old boy].
    Stasiowska-Saeid E
    Pediatr Pol; 1985 Sep; 60(9):667-70. PubMed ID: 3831901
    [No Abstract]   [Full Text] [Related]  

  • 7. Trisomy 20p: case report and genetic review.
    Lurie IW; Rumyantseva NV; Zaletajev DV; Gurevich DB; Korotkova IA
    J Genet Hum; 1985 Jan; 33(1):67-75. PubMed ID: 3981145
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Trisomy 13 in the child of two carriers of a 13/15 translocation.
    Mori MA; Huertas H; Pinel I; Giralt P; Martínez-Frías ML
    Am J Med Genet; 1985 Jan; 20(1):17-20. PubMed ID: 3970069
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Partial trisomy of the proximal part of the long arm of chromosome 13].
    Saura R; Longy M; Serville F; Sautarel M; Renouil M; Sandler B
    Pediatrie; 1982 Sep; 37(6):473-7. PubMed ID: 7155728
    [No Abstract]   [Full Text] [Related]  

  • 10. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
    García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM
    Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T; Acar H; Oran B
    Genet Couns; 2000; 11(1):25-32. PubMed ID: 10756424
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Unusual 13/13 translocation and 13 trisomy phenotype.
    Fryns JP; Kleczkowska A; Kubien E
    Ann Genet; 1982; 25(2):113-5. PubMed ID: 6984626
    [No Abstract]   [Full Text] [Related]  

  • 14. Partial trisomy and monosomy for short arm of chromosome number 5 in two sibs and a balanced translocation carrier father.
    Kulkarni MV; Patel ZM; Peter JJ; Ambani LM
    Indian Pediatr; 1981 Apr; 18(4):263-6. PubMed ID: 7287154
    [No Abstract]   [Full Text] [Related]  

  • 15. Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.
    Fujimoto A; Lin MS; Korula SR; Wilson MG
    Am J Med Genet; 1985 Oct; 22(2):333-42. PubMed ID: 4050866
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial trisomy 13 with phenotype of Patau syndrome due to maternal reciprocal translocation t(6;13) (q25;q13).
    Petit P; Fryns JP; van den Berghe H
    Ann Genet; 1980; 23(1):57-9. PubMed ID: 6965845
    [No Abstract]   [Full Text] [Related]  

  • 17. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA; Mikel'saar AV; Mikel'saar RV
    Sov Genet; 1974 Jun; 8(5):651-7. PubMed ID: 4413436
    [No Abstract]   [Full Text] [Related]  

  • 18. [Unusual clinical and cytogenetic findings in a child with trisomy 13 (46, XY, -13, +t (13q 13q))].
    Faschingbauer C; Ulmer R
    Padiatr Padol; 1983; 18(1):39-44. PubMed ID: 6835681
    [No Abstract]   [Full Text] [Related]  

  • 19. Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter.
    Pagano L; Fioretti G; Vetrella M; Risolo E; Casullo C; Celona A; Renda S; Rinaldi A; Ventruto V
    Ann Genet; 1980; 23(3):173-5. PubMed ID: 6968535
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Partial trisomy C by t(Cq-; Dp+) translocation with a C(p- q+) remnant].
    De Grouchy J; Thieffry S; Aicardi J; Chevrie JJ; Zucker G
    Arch Fr Pediatr; 1967 Oct; 24(8):859-68. PubMed ID: 5584189
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 4.