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 *

221 related articles for article (PubMed ID: 7228038)

  • 21. 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]  

  • 22. Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.
    Hobolth N; Jacobsen P; Mikkelsen M
    J Med Genet; 1974 Sep; 11(3):299-303. PubMed ID: 4139263
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
    Balci S; Aypar E; Beksaç MS; Bartsch O
    Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Familial translocation t(3;22) detected in a carrier child with mental retardation and other abnormalities].
    Gregori Romero M; Gil Benso R; López Ginés C; Pellín Pérez A; Barberá Guillem E
    An Esp Pediatr; 1984 Oct; 21(6):593-6. PubMed ID: 6524770
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Partial trisomy 8 (8q24) and the trisomy-8 syndrome.
    Sánchez O; Yunis JJ
    Humangenetik; 1974; 23(4):297-303. PubMed ID: 4420964
    [No Abstract]   [Full Text] [Related]  

  • 26. Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk.
    Stengel-Rutkowski S; Lohse K; Herzog C; Apacik C; Couturier J; Albert A; Belohradsky B
    Clin Genet; 1992 Oct; 42(4):178-85. PubMed ID: 1424241
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Partial trisomy 11q and familial translocation 11--22 (author's transl)].
    Giraud F; Mattei JF; Mattei MG; Bernard R
    Humangenetik; 1975 Aug; 28(4):343-7. PubMed ID: 1176125
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Banding identification of partial trisomy 15 and of 8/21 translocation.
    Wurster-Hill DH; Hoefnagel D
    J Ment Defic Res; 1974 Jun; 18(2):139-44. PubMed ID: 4141377
    [No Abstract]   [Full Text] [Related]  

  • 29. 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]  

  • 30. Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents.
    Ayme S; Mattei MG; Mattei JF; Giraud F
    Hum Genet; 1979 Apr; 48(1):7-12. PubMed ID: 457136
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21.
    Pfeiffer RA; Kessel EK; Soer KH
    Clin Genet; 1977 Mar; 11(3):207-13. PubMed ID: 138497
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A case of 21q-syndrome with half normal SOD-1 activity.
    Yoshimitsu K; Hatano S; Kobayashi Y; Takeoka Y; Hayashidani M; Ueda K; Nomura K; Ohama K; Usui T
    Hum Genet; 1983; 64(2):200-2. PubMed ID: 6885062
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Partial trisomy 2p.
    Pueschel SM; Scola PS; Mendoza T
    J Ment Defic Res; 1987 Sep; 31 ( Pt 3)():293-8. PubMed ID: 3681957
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A familial F/G translocation [t(p-; 22q+)] observed in three generations.
    Cohen MM; Davidson RG; Brown JA
    Clin Genet; 1975 Feb; 7(2):120-7. PubMed ID: 1132159
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Inherited partial duplication of chromosome No. 15.
    Fujimoto A; Towner JW; Ebbin AJ; Kahlstrom EJ; Wilson MG
    J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Banding identification of chromosomal abnormalities in four patients: ring (6), translocation (2q-;15q+), translocation (21q;21q) and deletion (22q-).
    Wurster-Hill DH; Hoefnagel D
    J Ment Defic Res; 1975 Jun; 19(2):145-50. PubMed ID: 127842
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Partial trisomy of chromosome 21 by maternal translocation t(15;21) (q26.2; q21)].
    Raoul O; Carpentier S; Dutrillaux B; Mallet R; Lejeune J
    Ann Genet; 1976 Sep; 19(3):187-90. PubMed ID: 136225
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Interchromosomal duplication for the short arm of chromosome no. 9: report of three cases due to a familial translocation t(9; 11) and one case with a de novo 47, XX, +9p karyotype.
    Lin CC; Holman G; Sewell L; Bowen P; Biederman B
    J Ment Defic Res; 1977 Dec; 21(4):309-29. PubMed ID: 604504
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [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]  

  • 40. Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations.
    Nakai H; Yamamoto Y; Kuroki Y
    Hum Genet; 1979 Oct; 51(3):349-55. PubMed ID: 511169
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.