BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

33 related articles for article (PubMed ID: 7436152)

  • 1. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A; Delicado A; Izquierdo M; Oliver A; López Pajares I; Gracia R; Peralta A
    An Esp Pediatr; 1981 May; 14(5):344-51. PubMed ID: 7294523
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of congenital adrenal hyperplasia.
    Marcus ES; Holcombe JH; Tulchinsky D; Rich RR; Riccardi VM
    Am J Med Genet; 1979; 4(2):201-4. PubMed ID: 517576
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISH.
    Delneste D; Vamos E; Pierquin G; Hayez-Delatte F; Van Regemorter N
    Genet Couns; 1998; 9(2):97-102. PubMed ID: 9664205
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)].
    Obry E; Piussan C; Risbourg B; Dutrillaux B
    Ann Genet; 1980; 23(4):216-20. PubMed ID: 6971599
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Autosomal translocation in gynaecology and obstetrics. 2. Cytogenetic findings (author's transl)].
    Weise W
    Zentralbl Gynakol; 1982; 104(6):329-42. PubMed ID: 7090638
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Balanced translocation 8:10 and adrenogenital syndrome. Family study (author's transl)].
    del Mazo J; Martín MJ; Abrisqueta JA; Aller V; Martín-Lucas MA; Pérez-Castillo A; de Torres ML
    An Esp Pediatr; 1980 Aug; 13(8):710-3. PubMed ID: 7436152
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Adrenogenital syndrome with 21-hydroxylase deficiency].
    Dörr HG; Sippell WG
    Monatsschr Kinderheilkd; 1993 Jul; 141(7):609-21. PubMed ID: 8413342
    [No Abstract]   [Full Text] [Related]  

  • 8. Human chromosome analysis: methodology and applications.
    Larson L
    Am J Med Technol; 1983 Oct; 49(10):687-98. PubMed ID: 6228140
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Chromosomal anomaly and mental deficiency. Study of one case of a ringed chromosome 15 (author's transl)].
    Benadiba M; Hamon J; Fausser C; Helmlinger W
    Neuropsychiatr Enfance Adolesc; 1981; 29(11-12):631-9. PubMed ID: 7045716
    [No Abstract]   [Full Text] [Related]  

  • 10. [Adrenogenital syndrome--molecular biology and prenatal diagnosis].
    Ohlsson G; Müller JR; Schwartz M
    Ugeskr Laeger; 1998 Feb; 160(6):803-7. PubMed ID: 9469975
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature.
    Ruiz C; Grubs RE; Jewett T; Cox-Jones K; Abruzzese E; Pettenati MJ; Rao PN
    Am J Med Genet; 1996 Aug; 64(3):478-84. PubMed ID: 8862625
    [TBL] [Abstract][Full Text] [Related]  

  • 12. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
    Legare JM; Sekhon GS; Laxova R
    Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 14.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 15.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.