BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 5643178)

  • 1. Familial occurrence of trisomy 22.
    Uchida IA; Ray M; McRae KN; Besant DF
    Am J Hum Genet; 1968 Mar; 20(2):107-18. PubMed ID: 5643178
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
    Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome.
    Weiss L; Wolf CB
    Am J Dis Child; 1968 Dec; 116(6):609-14. PubMed ID: 4235163
    [No Abstract]   [Full Text] [Related]  

  • 6. A patient with 45,XX,Gminus-46,XX,Gr mosaicism.
    Blank CE; Lorber J
    J Med Genet; 1969 Jun; 6(2):220-3. PubMed ID: 5801471
    [No Abstract]   [Full Text] [Related]  

  • 7. Structural abnormalities of chromosome 18. 3. Two G-18 translocations, one identified AS 22-18.
    Fraccaro M; Herin P; Hultén M; Ivemark BI; Jonasson J; Lindsten J; Tiepolo L; Zetterqvist P
    Ann Genet; 1972 Jun; 15(2):93-8. PubMed ID: 4537728
    [No Abstract]   [Full Text] [Related]  

  • 8. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
    Lejeune J; Rethoré MO; Berger R; Abonyi D; Dutrillaux B; See G
    Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617
    [No Abstract]   [Full Text] [Related]  

  • 9. [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].
    LEJEUNE J; BERGER R; RETHORE MO; ARCHAMBAULT L; JEROME H; THIEFFRY S; AICARDI J; BROYER M; LAFOURCADE J; CRUVEILLER J; TURPIN R
    C R Hebd Seances Acad Sci; 1964 Nov; 259():4187-90. PubMed ID: 14260664
    [No Abstract]   [Full Text] [Related]  

  • 10. [Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation].
    de Grouchy J; Emerit I; Aicardi J
    Ann Genet; 1969 Jun; 12(2):133-7. PubMed ID: 5308386
    [No Abstract]   [Full Text] [Related]  

  • 11. A case of familial chromosomal aberration with G group mosaic.
    Gedda L; Torrioli-Riggio G; Romei L; Alfieri A; Calabresi F; Del Porto G; Gentile R
    Acta Genet Med Gemellol (Roma); 1967 Jan; 16(1):8-20. PubMed ID: 6063938
    [No Abstract]   [Full Text] [Related]  

  • 12. A pedigree of 4/18 translocation chromosomes with type and countertype partial trisomy and partal monosomy for chromosome 18.
    Valdmanis A; Pearson G; Siegel AE; Hoeksema RH; Mann JD
    Ann Genet; 1967 Dec; 10(4):159-66. PubMed ID: 5301688
    [No Abstract]   [Full Text] [Related]  

  • 13. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A; Tenconi R; Baccichetti C; Pujatti G
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
    [No Abstract]   [Full Text] [Related]  

  • 14. Cat-eye syndrome, a partial trisomy 22.
    Bühler EM; Méhes K; Müller H; Stalder GR
    Humangenetik; 1972; 15(2):150-62. PubMed ID: 5049068
    [No Abstract]   [Full Text] [Related]  

  • 15. Trisomy 22: a clinical entity.
    Hsu LY; Shapiro LR; Gertner M; Lieber E; Hirschhorn K
    J Pediatr; 1971 Jul; 79(1):12-9. PubMed ID: 5091253
    [No Abstract]   [Full Text] [Related]  

  • 16. DOUBLE ANEUPLOIDY: TRISOMY 21 AND XO--XX SEX CHROMOSOME MOSAICISM.
    ROOT AW; BONGIOVANNI AM; BREIBART S; MELLMAN WJ
    J Pediatr; 1964 Dec; 65():937-9. PubMed ID: 14244103
    [No Abstract]   [Full Text] [Related]  

  • 17. [Clinical anatomic and histopathological study of ocular signs in 2 cases of mosaicism associated with autosomal 18-21 double trisomy].
    Laliam M; Laliam N; Ouadahi MS; Iles S; Ould Larbi L
    Bull Mem Soc Fr Ophtalmol; 1972; 85(0):83-90. PubMed ID: 4211332
    [No Abstract]   [Full Text] [Related]  

  • 18. Results of 538 chromosome studies on patients referred for cytogenetic analysis.
    Mulcahy MT; Jenkyn J
    Med J Aust; 1972 Dec; 2(24):1333-8. PubMed ID: 4265391
    [No Abstract]   [Full Text] [Related]  

  • 19. [A case of trisomy 21 (47, XX, 21 +) due to interchromosome effect].
    Fraisse J; Gannat B; La Selve A
    J Med Lyon; 1972 Feb; 53(223):235-6. PubMed ID: 5039271
    [No Abstract]   [Full Text] [Related]  

  • 20. A partial D-trisomy-normal mosaic female.
    Webb GC; Garson M; Robson MK; Pitt DB
    J Med Genet; 1971 Dec; 8(4):522-7. PubMed ID: 5149538
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.