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 *

151 related articles for article (PubMed ID: 1270083)

  • 1. [A girl with a deletion (2) (q34q36): cytogenetic and clinical observations (author's transl)].
    Warter S; Lausecker C; Pennerath A
    Hum Genet; 1976 May; 32(2):225-7. PubMed ID: 1270083
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Interstitial deletion of the long arm of chromosome 2: case report and review of literature.
    Taysi K; Dengler DR; Jones LA; Heersma JR
    Ann Genet; 1981; 24(4):245-7. PubMed ID: 7036843
    [No Abstract]   [Full Text] [Related]  

  • 3. [Monosomy 7qter (author's transl)].
    Turleau C; de Grouchy J; Perignon F; Lenoir G
    Ann Genet; 1979; 22(4):242-4. PubMed ID: 317790
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Ring chromosome 13 (author's transl)].
    Hevia A; Bullon M; Novales A; Fernandez-Novoa C; San Martin V; Galera H
    Ann Genet; 1979; 22(4):232-3. PubMed ID: 317788
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Interstitial deletion of chromosome 2q associated with ovarian dysgenesis.
    Davis E; Grafe M; Cunniff C; Jones KL; Bogart M
    Clin Genet; 1991 May; 39(5):386-90. PubMed ID: 1860256
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Holt-Oram syndrome with chromosomopathy (author's transl)].
    González Espinosa C; Artiles Pérez L; García Báez M; Otero Gómez A; García Miranda JL
    An Esp Pediatr; 1982 Jan; 16(1):77-81. PubMed ID: 7081854
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Trisomy 4p. A case presentation (author's transl)].
    Delgado A; Egüés J; Muñoz M; González Villa P; Bernaola E; del Amo A
    An Esp Pediatr; 1981 Oct; 15(4):383-9. PubMed ID: 7337304
    [No Abstract]   [Full Text] [Related]  

  • 8. [9p monosomy. About a new case. Clinical and cytogenetic study (author's transl)].
    Lajarrige C; Bouquier JJ; Ronayette D; Tchertoff C; Faugeras C; Barthe D; Laleu J
    Ann Pediatr (Paris); 1979 Nov; 26(9):631-6. PubMed ID: 555637
    [No Abstract]   [Full Text] [Related]  

  • 9. [Two new cases of partial monosomy 11q with breakpoint in 11q24 (author's transl)].
    Laurent C; Biemont MC; Veyron M; Guilhot J; Guibaud P
    Ann Genet; 1979; 22(4):239-41. PubMed ID: 317789
    [No Abstract]   [Full Text] [Related]  

  • 10. A patient with interstitial deletion 7 (p13 leads to p21).
    Müller U; Staudt F; Hameister H
    Ann Genet; 1981; 24(4):239-41. PubMed ID: 6800299
    [No Abstract]   [Full Text] [Related]  

  • 11. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J; Plaza J; Geán E
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Ring chromosome 6: case report and review of literature.
    Kini KR; Van Dyke DL; Weiss L; Logan MS
    Hum Genet; 1979; 50(2):145-9. PubMed ID: 511129
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [12 p trisomy. A new case (author's transl)].
    Kubryk N; Prieur M; Borde M
    Ann Pediatr (Paris); 1980 Dec; 27(10):695-9. PubMed ID: 7212558
    [No Abstract]   [Full Text] [Related]  

  • 14. Some clinical and cytogenetic observations on a ring chromosome 13 (p11 q34).
    Hernandez A; Garcia-Cruz D; Plascencia L; Nazara Z; Rivera H; Sanchez-Corona J; Cantu JM
    Ann Genet; 1979; 22(4):221-4. PubMed ID: 317785
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The clinical features of the 18 q-syndrome (author's transl)].
    Feichtinger C; Glatzl J
    Wien Klin Wochenschr; 1974 Aug; 86(15):441-4. PubMed ID: 4605988
    [No Abstract]   [Full Text] [Related]  

  • 16. Syndromes due to chromosomal abnormalities: partial trisomy 22, interstitial deletion of the long arm of 13, and trisomy 8.
    Pai GS; Thomas GH; Leonard CO; Ward JC; Valle DL; Pyeritz RE
    Johns Hopkins Med J; 1979 Oct; 145(4):162-9. PubMed ID: 491337
    [No Abstract]   [Full Text] [Related]  

  • 17. De novo interstitial deletion del(1)(p21p32).
    Bene M; Duca-Marinescu A; Ioan D; Maximilian C
    J Med Genet; 1979 Aug; 16(4):323-7. PubMed ID: 490590
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes.
    Park VM; Gustashaw KM; Bilenker RM; Golden WL
    Am J Med Genet; 1991 Nov; 41(2):180-3. PubMed ID: 1785630
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A girl with 46,XX,t(1;15) karyotype. Cytogenetic and clinical observations.
    van Hemel JO; van Biervliet JP; de Jager-van der Grift PW
    Clin Genet; 1975 Sep; 8(3):213-7. PubMed ID: 1175325
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.