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 *

225 related articles for article (PubMed ID: 7445073)

  • 1. [Interpretation of the karyotype characteristics of patients with developmental defects of the urogenital system].
    Kirillova EA; Rozovskiĭ IS
    Tsitol Genet; 1980; 14(1):55-9. PubMed ID: 7445073
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetic anomalies in dysmenorrhea and sterility: range and frequency, age-related dependence, mosaicism dynamics].
    Sazonova LA; Suskov II
    Genetika; 1983; 19(1):171-3. PubMed ID: 6682067
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [A clinical and cytogenetic investigation carried out in a special institution for mentally retarded patients: preliminary results concerning 82 cases of oligophrenia (author's transl)].
    Mounoud RL; Klein D; Bettschart W; Cabrol C
    J Genet Hum; 1976 Dec; 24(4):297-335. PubMed ID: 1022853
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic analysis of patients with developmental anomalies of the müllerian ducts.
    Capraro VJ; Cohen MM
    Obstet Gynecol; 1969 May; 33(5):647-8. PubMed ID: 5778444
    [No Abstract]   [Full Text] [Related]  

  • 5. A cytogenetic study of five rare karyotypes.
    Yang ZR; Xiao YZ; Liu XX
    J Tongji Med Univ; 1992; 12(4):234-6. PubMed ID: 1289572
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A case of juvenile chronic myeloid leukemia with XX/XXX mosaicism.
    Yeşilipek MA; Lüleci G; Oygür N; Berker S; Yegin O
    Turk J Pediatr; 1992; 34(4):251-4. PubMed ID: 1306346
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Gamete donor karyotyping: between real usefulness and safety rules].
    Siffroi JP;
    Gynecol Obstet Fertil; 2004 Sep; 32(9):803-12. PubMed ID: 15380766
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetics of müllerian agenesis. A case report.
    Jaffe SB; Loucopoulos A; Jewelewicz R
    J Reprod Med; 1992 Mar; 37(3):242-6. PubMed ID: 1564711
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals.
    Smith A; Collis J
    Med J Aust; 1983 Jul; 2(1):9-10. PubMed ID: 6865834
    [No Abstract]   [Full Text] [Related]  

  • 10. Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literature.
    Schubert R; Eggermann T; Hofstaetter C; von Netzer B; Knöpfle G; Schwanitz G
    Am J Med Genet; 2002 Jul; 110(3):278-82. PubMed ID: 12116238
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A clinical and cytogenetic study of Turner syndrome.
    Suri M; Kabra M; Jain U; Sanders V; Saxena R; Shukla A; Singh GV; Verma IC
    Indian Pediatr; 1995 Apr; 32(4):433-42. PubMed ID: 8635807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two unbalanced segregation products due to a maternal t(7;16)inv(16).
    Leegte B; Sikkema-Raddatz B; Hordijk R; Davelaar I; van der Veen A; Cobben JM
    Prenat Diagn; 2001 Jul; 21(7):550-2. PubMed ID: 11494289
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Familial pericentric inversion of chromosome 8 : is breakpoint p22q23 important in the formation of unbalanced recombinants?
    Moedjono SJ; Sparkes RS
    Ann Genet; 1980; 23(4):235-7. PubMed ID: 6971603
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tissue limited mosaicism for unbalanced autosomal translocation in a child with congenital anomalies and mental retardation.
    Summitt RL; Tharapel AT; Wilroy RS
    Eur J Pediatr; 1977 Jul; 125(3):169-74. PubMed ID: 885143
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mosaicism with a normal cell line and an unbalanced structural rearrangement.
    Zaslav AL; Fallet S; Blumenthal D; Jacob J; Fox J
    Am J Med Genet; 1999 Jan; 82(1):15-9. PubMed ID: 9916836
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization.
    Robson L; Jackson J; Cowell C; Sillence D; Smith A
    Am J Med Genet; 1994 Apr; 50(3):251-4. PubMed ID: 8042669
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Pericentric inversion of chromosome 9 in two women with developmental defects of the internal genitalia].
    Kirillova EA; Rozovskiĭ IS; Kurbanova AG; Karetnikova NA
    Tsitol Genet; 1979; 13(4):300-4. PubMed ID: 516157
    [No Abstract]   [Full Text] [Related]  

  • 19. [Clinical polymorphism in amenorrhea of chromosomal and nonchromosomal etiologies].
    Kirillova EA; Kaurov BA; Konstantinova LM
    Genetika; 1988 Aug; 24(8):1470-7. PubMed ID: 3060400
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosage.
    Maraschio P; Danesino C; Lo Curto F; Zuffardi O; Dalla Fior T; Pedrotti D
    Ann Genet; 1984; 27(2):96-101. PubMed ID: 6331797
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.