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 *

166 related articles for article (PubMed ID: 6570667)

  • 1. [Genetics and genetic diseases (V)].
    Xu WH
    Zhonghua Hu Li Za Zhi; 1984 Oct; 19(5):305-9. PubMed ID: 6570667
    [No Abstract]   [Full Text] [Related]  

  • 2. "Genetic for medical practitioners".
    Ambani LM
    Q Med Rev; 1981 Oct; 32(4):1-43. PubMed ID: 7051087
    [No Abstract]   [Full Text] [Related]  

  • 3. [Current methods of chromosome studies].
    Simola KO
    Duodecim; 1986; 102(20):1545-53. PubMed ID: 3769837
    [No Abstract]   [Full Text] [Related]  

  • 4. [Current problems of clinical genetics].
    Davidenkova EF
    Vestn Akad Med Nauk SSSR; 1976; (7):68-76. PubMed ID: 1027303
    [No Abstract]   [Full Text] [Related]  

  • 5. Chromosomal abnormalities ascertained in the collaborative perinatal survey of 7- and 8-year-old children.
    Lubs HA; Patil SR; Kimberling WJ; Brown J; Cohen MM; Gerald PS; Hecht F; Moorhead P; Myrianthopoulos NC; Summit RL
    Birth Defects Orig Artic Ser; 1979; 15(1):191-202. PubMed ID: 444641
    [No Abstract]   [Full Text] [Related]  

  • 6. [Studies of the chromosome pattern in Stein-Leventhal syndrome].
    Lezhava TA
    Tsitologiia; 1966; 8(2):221-9. PubMed ID: 5984071
    [No Abstract]   [Full Text] [Related]  

  • 7. Application of new technics of chromosome identification to cytogenetic problems.
    Borgaonkar DS
    Birth Defects Orig Artic Ser; 1973 Jan; 9(1):171-82. PubMed ID: 4120145
    [No Abstract]   [Full Text] [Related]  

  • 8. [Cytogenetics in pediatric practice. Experience of 10 years (author's transl)].
    Carnevale A; Blanco B; Frías S; Castillo J; Vázquez V
    Rev Invest Clin; 1981; 33(2):175-81. PubMed ID: 7291763
    [No Abstract]   [Full Text] [Related]  

  • 9. [Chromosomal diseases in children].
    Demidova IA
    Med Sestra; 1988 Sep; 47(9):31-4. PubMed ID: 3205133
    [No Abstract]   [Full Text] [Related]  

  • 10. The mutation rate in man.
    Edwards JH
    Prog Med Genet; 1974; 10():1-16. PubMed ID: 4620173
    [No Abstract]   [Full Text] [Related]  

  • 11. [Significance of chromosome analysis in habitual abortion].
    Gabriel D; Weise W
    Zentralbl Gynakol; 1983; 105(8):510-5. PubMed ID: 6683453
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Proportion of abnormal karyotypes found in chromosome studies for abnormal phenotypes].
    Kosztolányi G
    Orv Hetil; 1987 Aug; 128(33):1711-5. PubMed ID: 3627778
    [No Abstract]   [Full Text] [Related]  

  • 13. Recent advances in genetics.
    Blitzer MG; Schwartz S; Cowan TM; Raffel LJ
    Md Med J; 1989 Nov; 38(11):917-24. PubMed ID: 2685498
    [No Abstract]   [Full Text] [Related]  

  • 14. A chromosomal survey of an institution for the mentally retarded. Study of 476 karyotypes with banding techniques and clinical assessment of patients with chromosome anomalies.
    Nielsen KB; Dyggve HV; Knudsen H; Olsen J
    Dan Med Bull; 1983 Feb; 30(1):5-13. PubMed ID: 6831943
    [No Abstract]   [Full Text] [Related]  

  • 15. [Chromosome anomalies and genetics].
    Higurashi M; Matsui I; Naganuma M
    Naika; 1969 Apr; 23(4):633-7. PubMed ID: 5800501
    [No Abstract]   [Full Text] [Related]  

  • 16. [Indications of chromosome and DNA analysis for the diagnosis of genetic diseases].
    Romana SP; Gérard B
    Rev Prat; 1997 Jun; 47(11):1241-52. PubMed ID: 9238821
    [No Abstract]   [Full Text] [Related]  

  • 17. Elusive chromosome anomalies.
    Francke U
    Hosp Pract (Off Ed); 1986 May; 21(5):175-8, 182, 191-3. PubMed ID: 3084511
    [No Abstract]   [Full Text] [Related]  

  • 18. Genetics: your fate in your genes.
    Matthews DR
    Nurs Mirror; 1978 Oct; 147(15):30-4. PubMed ID: 250094
    [No Abstract]   [Full Text] [Related]  

  • 19. [Palmar ridge count. Heredity and clinical applications].
    Benigno V; Di Peri S; Boncori R; Como G; Distefano F
    Minerva Pediatr; 1988 May; 40(5):259-64. PubMed ID: 3173277
    [No Abstract]   [Full Text] [Related]  

  • 20. Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1).
    Wiktor A; Van Dyke DL; Weiss L
    Am J Med Genet; 1993 Jan; 45(1):22-4. PubMed ID: 8418653
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.