BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 3587191)

  • 1. [Brachmann-Cornelia de Lange syndrome].
    Bonioli E; Bellini C; Ruffa G; Camera G; Gemme G
    Minerva Pediatr; 1987 Feb; 39(3-4):135-8. PubMed ID: 3587191
    [No Abstract]   [Full Text] [Related]  

  • 2. [Brachmann-de Lange syndrome: report of 4 cases in Mexican children].
    Villegas-Camargo I; Lacro RV; Lyons-Jones K
    Bol Med Hosp Infant Mex; 1987 Dec; 44(12):766-70. PubMed ID: 3426781
    [No Abstract]   [Full Text] [Related]  

  • 3. Orofaciodigital syndrome type IV: report of a patient.
    Nevin NC; Thomas PS
    Am J Med Genet; 1989 Feb; 32(2):151-4. PubMed ID: 2929654
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Terminal deletion of the short arm of chromosome 3.
    Lizcano-Gil LA; Figuera LE
    Genet Couns; 1994; 5(1):35-8. PubMed ID: 8031533
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The Mohr syndrome (orofaciodigital syndrome type II). 1 familial case].
    Cotton JB; Gardet R; Ladreyt JP; Guibaud P
    Pediatrie; 1979; 34(3):257-66. PubMed ID: 492868
    [No Abstract]   [Full Text] [Related]  

  • 6. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].
    Ayral D; Raudrant D; Charleux JP; Noel B
    Pediatrie; 1984 Dec; 39(8):681-90. PubMed ID: 6598632
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.
    Ireland M; English C; Cross I; Houlsby WT; Burn J
    J Med Genet; 1991 Sep; 28(9):639-40. PubMed ID: 1956066
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Papillon-Lége and Psaume orofaciodigital syndrome (OFD syndrome)].
    Felgenhauer WR; Farquet M; Ferrier PE
    Arch Genet (Zur); 1972; 45(2):65-87. PubMed ID: 4657589
    [No Abstract]   [Full Text] [Related]  

  • 9. Robert's syndrome.
    Shah SB; Deshpande VS; Kalyani R; Patel DN
    Indian Pediatr; 1984 Jun; 21(6):500-2. PubMed ID: 6511080
    [No Abstract]   [Full Text] [Related]  

  • 10. A contribution to the genetics of oral-facial-digital (OFD) syndrome.
    Chaurasia BD; Goswami HK
    Jinrui Idengaku Zasshi; 1973 Dec; 18(3):294-9. PubMed ID: 4800018
    [No Abstract]   [Full Text] [Related]  

  • 11. Partial duplication of 3q (q25.1-->q26.1) without the Brachmann-de Lange phenotype.
    Lopez-Rangel E; Dill FJ; Hrynchak MA; Van Allen MI
    Am J Med Genet; 1993 Nov; 47(7):1068-71. PubMed ID: 8291525
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The 4p- syndrome. A clinically recognizable chromosomal deletion syndrome.
    Guthrie RD; Aase JM; Asper AC; Smith DW
    Am J Dis Child; 1971 Nov; 122(5):421-5. PubMed ID: 5129531
    [No Abstract]   [Full Text] [Related]  

  • 13. Trisomy 18 (Edwards syndrome) in Delaware.
    Morallo LM; Rosenblum H; Esterly KL; Johnson WD; Storlazzi JJ; Narvaez AC; Borgaonkar DS
    Del Med J; 1983 Jan; 55(1):27-30. PubMed ID: 6840358
    [No Abstract]   [Full Text] [Related]  

  • 14. [Wolf syndrome. Apropos of 2 cases].
    García González P; Pedraz García C; Merino Marcos L; Salazar Veloz J; Escudero Bueno G; Salazar Villalobos V
    An Esp Pediatr; 1983 Feb; 18(2):113-7. PubMed ID: 6881733
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of interstitial deletion of 17(p11.2p11.2) (Smith-Magenis syndrome).
    Fan YS; Farrell SA
    Am J Med Genet; 1994 Jan; 49(2):253-4. PubMed ID: 8116679
    [No Abstract]   [Full Text] [Related]  

  • 16. Partial deletion of the short arm of a chromosome No. 4. Wolf's syndrome.
    van Kempen C; Jongbloet PH
    Maandschr Kindergeneeskd; 1967 Oct; 35(8):252-69. PubMed ID: 6065161
    [No Abstract]   [Full Text] [Related]  

  • 17. [Diagnosis and prevention of chromosome aberrations].
    Sachs ES; van Hemel JO
    Ned Tijdschr Geneeskd; 1982 Dec; 126(49):2236-44. PubMed ID: 6217426
    [No Abstract]   [Full Text] [Related]  

  • 18. [A case of neonatal Pallister-Killian syndrome (tetrasomy 12p)].
    González de Dios J; García-Alix Pérez A; Díaz de Bustamante A; Delicado Navarro A; Arés Segura S; Salas Hernández S; Quero Jiménez J
    An Esp Pediatr; 1993 Mar; 38(3):277-9. PubMed ID: 8460851
    [No Abstract]   [Full Text] [Related]  

  • 19. [OFD syndrome in a male. Clinical-genetic analysis of 33 families].
    Segni G; Serra A; Mastrangelo R; Polidori G; Massasso J
    Acta Genet Med Gemellol (Roma); 1970 Oct; 19(4):546-66. PubMed ID: 5512530
    [No Abstract]   [Full Text] [Related]  

  • 20. Oral-facial-skeletal syndromes.
    Neri G; Gurrieri F; Genuardi M
    Am J Med Genet; 1995 Nov; 59(3):365-8. PubMed ID: 8599363
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.