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 *

104 related articles for article (PubMed ID: 5173157)

  • 1. Abnormalities of human autosomes. I. Ambigous genitalia associated with a translocation 46,XY, t(Cq+;Cq-).
    German J; Simpson JL
    Birth Defects Orig Artic Ser; 1971 May; 7(6):145-9. PubMed ID: 5173157
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [C-G translocation: karyotype 46, XY,t(Cq-; Gq+): parents 46, XX and 46, XY].
    Lambotte C; Carlier G; Frederic J; Keutgen J
    Acta Paediatr Belg; 1971; 25(2):119-26. PubMed ID: 5565831
    [No Abstract]   [Full Text] [Related]  

  • 3. Balanced translocations involving chromosome 12: report of a case and possible evidence for position effect.
    Biederman B; Bowen P
    Ann Genet; 1976 Dec; 19(4):257-60. PubMed ID: 1087856
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ambiguous genitalia and mental retardation associated with a translocation 46, XX, t(9; 10) and a deletion in 9q.
    Jenkins EC; Chaganti RS; Wilbur L; German J
    Birth Defects Orig Artic Ser; 1976; 12(5):169-73. PubMed ID: 953219
    [No Abstract]   [Full Text] [Related]  

  • 5. [Translocation 46,XY,t(2;5) (q37;q14) and mental retardation. Clinical and cytogenetic study].
    Gilgenkrantz S; Walbaum R; Mauuary G; Pierson M
    J Genet Hum; 1976 Mar; 24(1):27-37. PubMed ID: 58967
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. A family with a presumptive C-F translocation in five generations.
    Therkelsen AJ; Klinge T; Henningsen K; Mikkelsen M; Schmidt G
    Ann Genet; 1971 Mar; 14(1):13-21. PubMed ID: 5314290
    [No Abstract]   [Full Text] [Related]  

  • 8. De novo complex chromosomal rearrangement (CCR) in a severely mentally retarded boy.
    Fryns JP; Kleczkowska A; Kenis H
    Ann Genet; 1984; 27(1):62-4. PubMed ID: 6609678
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Trisomy 10 p. Apropos of a case caused by a maternal translocation].
    Stoll C; Willard D
    Pediatrie; 1980; 35(3):251-5. PubMed ID: 7393692
    [No Abstract]   [Full Text] [Related]  

  • 10. Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13.
    Turleau C; de Grouchy J; Dufier JL; Phuc LH; Schmelck PH; Rappaport R; Nihoul-Fékété C; Diebold N
    Hum Genet; 1981; 57(3):300-6. PubMed ID: 6114032
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Partial trisomy 12p. A newborn child with karyotype 46,XY,der(11), t(11; 12) (q25; p11) mat. Case report and review.
    Ottolina de Bracamonte N; Velazco JQ; Hammond Figueroa FG
    Acta Cient Venez; 1982; 33(4):342-7. PubMed ID: 7186725
    [No Abstract]   [Full Text] [Related]  

  • 12. Monosomy 7 syndrome associated with congenital adrenal hypoplasia and male pseudohermaphroditism.
    Le SQ; Kutteh WH
    Obstet Gynecol; 1996 May; 87(5 Pt 2):854-6. PubMed ID: 8677114
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An unbalanced karyotype in a translocation (Cq-,Aq+) pedigree.
    Smith GF; Shear CS; Jalowayski I; Akesson HO
    J Ment Defic Res; 1969 Jun; 13(2):123-9. PubMed ID: 5794286
    [No Abstract]   [Full Text] [Related]  

  • 14. [Ring chromosome 6. Karotype 46, XY, r (6)-45, XY,-6].
    Van den Berghe H; Fryns JP; Cassiman JJ; David G
    Ann Genet; 1974 Mar; 17(1):29-35. PubMed ID: 4546343
    [No Abstract]   [Full Text] [Related]  

  • 15. Isochromosome-formation in chromosome 9.
    Miller K; Arslan-Kirchner M
    Ann Genet; 1994; 37(2):78-81. PubMed ID: 7985983
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Repeated early spontaneous abortions and maternal autosomal translocation t(Bq+, Cq-). Apropos of a case].
    Broustet A; Philippe E; Meli-Fournial AM; Amouretti M; Garcia J
    Bord Med; 1972 Mar; 5(6):669-72. PubMed ID: 5066287
    [No Abstract]   [Full Text] [Related]  

  • 17. [A case of C-D translocation in a 9 year old boy and his mother].
    Revazov AA; Russkikh VV
    Tsitologiia; 1966; 8(2):269-76. PubMed ID: 5984073
    [No Abstract]   [Full Text] [Related]  

  • 18. Male pseudohermaphroditism in sibs with the alpha-thalassemia/mental retardation (ATR-X) syndrome.
    Reardon W; Gibbons RJ; Winter RM; Baraitser M
    Am J Med Genet; 1995 Jan; 55(3):285-7. PubMed ID: 7726224
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
    Aledo AG; Gracia R; López Pajares I; González M; Oliver A; Peralta A
    An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Duplication 6q24 leads to 6qter in an infant from a balanced paternal translocation.
    Chase TR; Jalal SM; Martsolf JT; Wasdahl WA
    Am J Med Genet; 1983 Feb; 14(2):347-51. PubMed ID: 6837629
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.