BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 4745566)

  • 1. [Partial B trisomy in cat-cry-syndrome (author's transl)].
    Schwingshackl A; Ganner E
    Padiatr Padol; 1973; 8(4):362-71. PubMed ID: 4745566
    [No Abstract]   [Full Text] [Related]  

  • 2. Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocation.
    Leisti J; Kaback MM; Rimoin DL
    Birth Defects Orig Artic Ser; 1975; 11(5):317-9. PubMed ID: 1218232
    [No Abstract]   [Full Text] [Related]  

  • 3. The larynx in the cri du chat (cat cry) syndrome.
    Ward PH; Engel E; Nance WE
    Laryngoscope; 1968 Oct; 78(10):1716-33. PubMed ID: 5681688
    [No Abstract]   [Full Text] [Related]  

  • 4. [Reverse type of cri du chat disease: 5 p trisomy].
    Stoll C; Rethore MO; Laurent C; Lejeune J
    Arch Fr Pediatr; 1975; 32(6):551-61. PubMed ID: 1180635
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Partial monosomy and trisomy 5 p due to balanced translocation t (3,5) in the father (author's transl)].
    Andrle M; Erlach A; Rett A
    Wien Klin Wochenschr; 1981 Jan; 93(1):16-9. PubMed ID: 7222705
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A 45,XX,-5,-14,+t(5q;14q)mat cri du chat child.
    Bass HN; Sparkes RS; Crandall BF; Galos KJ; Howard J
    Ann Genet; 1978 Mar; 21(1):56-9. PubMed ID: 308345
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Familial occurrence of the cat's cry (cri du chat) syndrom resulting from a balanced t(5 : 12) translocation (author's transl)].
    Mazurczak T; Stolarska A; Sito A; Mataszewska K
    Probl Med Wieku Rozwoj; 1977; 7():169-77. PubMed ID: 614567
    [No Abstract]   [Full Text] [Related]  

  • 8. Wolf-Hirschhorn and Cri du Chat syndromes resulting from familial translocations: 3 further examples of the Bp monosomy epistatic effect.
    Petit P; Fryns JP
    Genet Couns; 1990; 1(2):179-84. PubMed ID: 2081002
    [TBL] [Abstract][Full Text] [Related]  

  • 9. "Cri du chat" syndrome with maternal insertional translocation.
    Berger R; Touati G; Derre J; Ortiz MA; Martinetti J
    Clin Genet; 1974; 5(5):428-32. PubMed ID: 4368036
    [No Abstract]   [Full Text] [Related]  

  • 10. [Familial segregation of a t(5p-;13q+). Complementary analysis from specimens preserved in liquid nitrogen].
    Carpentier S; Dutrillaux B; Lafourcade J; Berger R; Rethoré MO; Lejeune J
    Ann Genet; 1972 Mar; 15(1):57-60. PubMed ID: 4537617
    [No Abstract]   [Full Text] [Related]  

  • 11. A case of the "cri du chat" syndrome with an unusual karyotype in the father.
    Bogomazov EA; Aver'yanov YN; Zotov VV; Lur'e IV; Pavlyuk GI
    Sov Genet; 1974 Nov; 9(1):129-31. PubMed ID: 4453856
    [No Abstract]   [Full Text] [Related]  

  • 12. Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation.
    Gencik A; Gencikova A; Pálova A
    Acta Paediatr Acad Sci Hung; 1982; 23(3):291-8. PubMed ID: 7180435
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Rare developmental anomalies in children: 1) the cri du chat syndrome, karyotype: 46, XY, DEL (5) (P31); 2) the mixed type of syndrome with signs of Patau's syndrome and the cri du chat syndrome, karyotype: 46, XY, DER (5) T (5, 13) (P14, Q14) MAT].
    Badalian LO; Malygina NA; Mutovin GR; Petrukhin AS; Nikonov VP
    Pediatriia; 1980 Mar; (3):74-7. PubMed ID: 7375280
    [No Abstract]   [Full Text] [Related]  

  • 14. [Cri-du-chat syndrome and trisomy 8p due to a paternal translocation t(5;8)(p1409;p12)].
    Rethoré MO; Couturier J; Villain E; Hambourg M; Lejeune J
    Ann Genet; 1984; 27(2):118-21. PubMed ID: 6331789
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cat cry syndrome.
    Ito Y; Goto H
    Tohoku J Exp Med; 1967 Apr; 91(4):349-54. PubMed ID: 6069328
    [No Abstract]   [Full Text] [Related]  

  • 16. De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation.
    Chaganti RS; Morillo-Cucci G; Friis L; Degnan M; German J
    Ann Genet; 1976 Mar; 19(1):43-8. PubMed ID: 1084121
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cri du chat syndrome [46, XY, 5p-] with balanced B/F translocation in father and grandfather: a case report.
    Char F
    Birth Defects Orig Artic Ser; 1974; 10(10):49-53. PubMed ID: 4462641
    [No Abstract]   [Full Text] [Related]  

  • 18. The larynx in the cri du chat (cat cry) syndrome.
    Ward PH; Engel E; Nance WE
    Trans Am Acad Ophthalmol Otolaryngol; 1968; 72(1):90-102. PubMed ID: 5637525
    [No Abstract]   [Full Text] [Related]  

  • 19. [G-binding patterns of B group chromosome in 4 cases with 46, Bp (author's transl)].
    Tanigawa U; Tsuda K; Fujita H; Hirano Y
    Jinrui Idengaku Zasshi; 1974 Jun; 19(1):77. PubMed ID: 4476858
    [No Abstract]   [Full Text] [Related]  

  • 20. [Importance of the denaturation method in the explanation of unusual chromosomal translocations].
    Zergollern L; Beer Z; Muzinić D
    Acta Med Iugosl; 1974; 28(3):255-67. PubMed ID: 4848921
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.