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 *

184 related articles for article (PubMed ID: 316670)

  • 1. An infant with trisomy 9pter yields 9q22 resulting from 3:1 segregation in a 46,XX t(1;9) (p36;q22) mother.
    Neu RL; Dennis NR; Lanman JT; Bannerman RM
    Ann Genet; 1979; 22(3):151-4. PubMed ID: 316670
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
    Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM
    Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial translocation 2;17 with partial trisomy 2q32 leads to 2qter.
    Giliberti P; Celona A; Della Pietra M; De Masi RV; Fioretti G; Pagano L; Renda S; Vetrella A; Ventruto V
    Ann Genet; 1980; 23(4):249-50. PubMed ID: 6971607
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z; Mihci E; Keser I; Karaali K; Berker S; Luleci G
    Genet Couns; 2012; 23(2):239-47. PubMed ID: 22876583
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J; Chernos J; Roland B
    Am J Med Genet; 1997 Dec; 73(3):327-9. PubMed ID: 9415693
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
    Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG
    Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725
    [No Abstract]   [Full Text] [Related]  

  • 9. Proximal 14 trisomy 46,XX, -22 +der(14)t(14;22) (q21;q11)mat.
    Fried K; Goldberg MD; Rosenblatt M
    Teratology; 1980 Jun; 21(3):309-12. PubMed ID: 7455919
    [No Abstract]   [Full Text] [Related]  

  • 10. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V
    Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734
    [No Abstract]   [Full Text] [Related]  

  • 11. [Trisomy 9p. A case of translocation t(9;22) (p11;p11)mat in a little girl].
    Genest P; Roussy J; Genest FB; Dumas L
    Union Med Can; 1977 Jul; 106(7):956-9. PubMed ID: 898406
    [No Abstract]   [Full Text] [Related]  

  • 12. Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
    Taysi K; Chao WT; Monaghan N; Monaco MP
    Ann Genet; 1983; 26(4):243-6. PubMed ID: 6364954
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Duplication 16q12----qter arising from 3:1 segregation in a 46,XX,t(13;16) (q12;q12) mother.
    Pérez-Castillo A; Martin-Lucas MA; Abrisqueta JA
    Ann Genet; 1990; 33(2):121-3. PubMed ID: 2241087
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Rethoré syndrome (9p trisomy) with unusual karyotype: 46,XX,-9, + der 9p, t(9;9)mat].
    Di Cesare D; Paludetto R; Casullo C; Pagano L; Stabile M; Sicolo A; Ventruto V
    Minerva Pediatr; 1980 Dec; 32(23):1349-52. PubMed ID: 7219376
    [No Abstract]   [Full Text] [Related]  

  • 15. Duplication 11 (q22----qter) in an infant. A case report with review.
    Greig F; Rosenfeld W; Verma RS; Babu KA; David K
    Ann Genet; 1985; 28(3):185-8. PubMed ID: 3879155
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Adjacent-2 disjunction of a maternal t(9;22) leading to duplication 9pter----q22 and deficiency of 22pter----q11.2.
    Pivnick EK; Wilroy RS; Summitt JB; Tucker B; Herrod HG; Tharapel AT
    Am J Med Genet; 1990 Sep; 37(1):92-6. PubMed ID: 2240050
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction.
    Zackai EH; Emanuel BS
    Am J Med Genet; 1980; 7(4):507-21. PubMed ID: 7211960
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Abnormal chromosome 9 in a neonate program. Report of three cases.
    Nakamura Y; Sato E; Sakai K; Sakuma S; Hashimoto T; Sindou S
    Arch Pathol Lab Med; 1990 Feb; 114(2):185-7. PubMed ID: 2302035
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Reciprocal syndromes caused by deficiency duplication resulting from maternal t(10;18)(p12;q22) translocation].
    Rethoré MO; Prieur M; de Blois MC; Naffah J; Ravel A; Villain E; Lejeune J
    Ann Genet; 1985; 28(3):149-53. PubMed ID: 3879147
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].
    Siffroi JP; Romani F; Viguié F; Lejeune C
    Ann Genet; 1984; 27(4):241-4. PubMed ID: 6335372
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.