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 *

147 related articles for article (PubMed ID: 4142949)

  • 1. A possible case of partial trisomy for chromosome 22: further evidence from Giemsa banding studies.
    Sands ME
    J Ment Defic Res; 1974 Dec; 18(4):327-30. PubMed ID: 4142949
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. [Identification of numerical and structural anomalies of human G-group-chromosomes using the pankreatin-Giemsa-Banding-pattern].
    Müller W; Rosenkranz W
    Klin Padiatr; 1972 Jul; 184(4):265-71. PubMed ID: 4117041
    [No Abstract]   [Full Text] [Related]  

  • 4. Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.
    Neu RL; Ortega CC; Barg GA; Pinto W; Gardner LI; Howell WM; Denton TE
    J Med Genet; 1976 Dec; 13(6):520-2. PubMed ID: 65472
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Updating advances in cytogenetics. Applications of the new chromosome banding methods.
    Breg WR
    Birth Defects Orig Artic Ser; 1974; 10(8):7-18. PubMed ID: 4142402
    [No Abstract]   [Full Text] [Related]  

  • 6. An inherited translocation t(4;15) (p16;q22) leading to two cases of partial trisomy 15.
    Cohen MM; Ornoy A; Rosenmann A; Kohn G
    Ann Genet; 1975 Jun; 18(2):99-103. PubMed ID: 1081372
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Banding analysis of abnormal karyotypes in spontaneous abortion.
    Kajii T; Oama K; Niikawa N; Ferrier A; Avirachan S
    Am J Hum Genet; 1973 Sep; 25(5):539-47. PubMed ID: 4741848
    [No Abstract]   [Full Text] [Related]  

  • 8. New techniques in the study of human chromosomes: methods and applications.
    Dutrillaux B; Lejeune J
    Adv Hum Genet; 1975; 5():119-56. PubMed ID: 48327
    [No Abstract]   [Full Text] [Related]  

  • 9. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
    Obry E; Piussan C; Risbourg B; Dutrillaux B
    Ann Genet; 1980; 23(4):216-20. PubMed ID: 6971599
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [Partial trisomy 11q;22q (author's transl)].
    Benítez J; Ayuso C; García Aparicio J; Sáez E; Pérez Sotelo A; Bello MJ
    An Esp Pediatr; 1981 Sep; 15(3):293-300. PubMed ID: 7332142
    [No Abstract]   [Full Text] [Related]  

  • 12. Autosomal syndromes.
    Summitt RL
    Pediatr Ann; 1978 Jun; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
    [No Abstract]   [Full Text] [Related]  

  • 13. [Trisomy 10p as a result of familial 10/22 translocation].
    Zergollern L; Begovic D; Muzinić D
    Acta Med Iugosl; 1980; 34(2):113-22. PubMed ID: 7405617
    [No Abstract]   [Full Text] [Related]  

  • 14. [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]  

  • 15. A familial 10/13 translocation: partial trisomy C in an infant associated with familial 10/13 translocation.
    Mulcahy MT; Jenkyn J; Masters PL
    Clin Genet; 1974; 6(5):335-40. PubMed ID: 4434650
    [No Abstract]   [Full Text] [Related]  

  • 16. The trisomy 21 and the trisomy 17-18 syndromes in siblings.
    Holmgren G; Anséhn S
    Hum Hered; 1971; 21(6):577-9. PubMed ID: 5149963
    [No Abstract]   [Full Text] [Related]  

  • 17. [Familial translocation t(6; 18) (q16; q16; q23) with free 21 trisomy].
    Tenconi R; Baccichetti C; Dussini N; Panizza G
    Ann Genet; 1974 Dec; 17(4):275-7. PubMed ID: 4281288
    [No Abstract]   [Full Text] [Related]  

  • 18. [Phenotype and karyotype interrelationships in chromosomal diseases].
    Prokof'eva-Bel'govska ; Grinberg KN; Revazov AA; Mikel'saar AV; Kuliev AM
    Vestn Akad Med Nauk SSSR; 1973; 28(1):37-44. PubMed ID: 4797784
    [No Abstract]   [Full Text] [Related]  

  • 19. 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]  

  • 20. [T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter].
    Laurent C; Dutrillaux B; Biemont MC; Genoud J; Bethenod M
    Ann Genet; 1973 Dec; 16(4):281-4. PubMed ID: 4544094
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.