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: 7133872)

  • 1. [Computerized diagnosis of syndrome of multiple congenital developmental defects].
    Cherstvoĭ ED; Laziuk GI; Krasnoproshin VV; Obraztsov VA
    Pediatriia; 1982 Jul; (7):41-3. PubMed ID: 7133872
    [No Abstract]   [Full Text] [Related]  

  • 2. [CNS pathology in hereditary syndromes of congenital developmental defects].
    Ostrovskaia TI
    Arkh Patol; 1985; 47(10):42-8. PubMed ID: 3840990
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The pallister mosaic syndrome.
    Pallister PD; Meisner LF; Elejalde BR; Francke U; Herrmann J; Spranger J; Tiddy W; Inhorn SL; Opitz JM
    Birth Defects Orig Artic Ser; 1977; 13(3B):103-110. PubMed ID: 890087
    [No Abstract]   [Full Text] [Related]  

  • 4. [Approach to differential diagnosis of clinically related forms of chromosomal pathology using computers].
    Antonenko VG; Levina LIa; Konstantinova LM; Zaiarnyĭ AN
    Pediatriia; 1991; (10):25-9. PubMed ID: 1787996
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Developmental anomaly resembling the trisomy 18 syndrome.
    Simpson JL; German J
    Ann Genet; 1969 Jun; 12(2):107-10. PubMed ID: 5308380
    [No Abstract]   [Full Text] [Related]  

  • 6. A practical application of fluorescent in situ hybridization to the Wolf-Hirschhorn syndrome.
    Fagan K; Colley P; Partington M
    Pediatrics; 1994 May; 93(5):826-7. PubMed ID: 8165089
    [No Abstract]   [Full Text] [Related]  

  • 7. Prenatal diagnosis of urinary tract abnormalities--ultrasound and laboratory assessment to predict fetal outcome.
    Antsaklis AJ; Papantoniou NE; Varvarigos JE; Rodolakis AJ; Mesogitis SJ; Aravantinos ID
    Prog Clin Biol Res; 1989; 305():19-23. PubMed ID: 2668972
    [No Abstract]   [Full Text] [Related]  

  • 8. [A fatal autosomal recessive syndrome with multiple congenital contractures].
    Herva R; Leisti J; Kirkinen P; Seppänen U; Martikainen J
    Duodecim; 1985; 101(8):756-62. PubMed ID: 4039655
    [No Abstract]   [Full Text] [Related]  

  • 9. Ring chromosome 15 syndrome.
    Fryns JP; Jaeken J; Devlieger H; Debucquoy P; Eggermont E; Van den Berghe H
    Acta Paediatr Belg; 1981; 34(1):47-9. PubMed ID: 7270144
    [No Abstract]   [Full Text] [Related]  

  • 10. [Computerized analysis in the study of multiple congenital defects connected with chromosome abnormalities: phenotype-karyotypic relations and genetic markers].
    Ivanov VI; Levina LIa; Konstantinova LM; Zaiarnyĭ AN; Antonenko VG
    Vestn Ross Akad Med Nauk; 1992; (4):24-30. PubMed ID: 1384873
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Polymalformation syndrome.
    Vander Elst A
    J Belge Radiol; 1989 Dec; 72(6):528-9. PubMed ID: 2695526
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Short stature and language delay in a 5-year-old girl: 18p- syndrome.
    Grush ML; Kimberling WJ; Lynch HT
    Nebr Med J; 1982 Sep; 67(9):261-3. PubMed ID: 7133223
    [No Abstract]   [Full Text] [Related]  

  • 14. [A mosaic of ring chromosome 18].
    Srsen S; Volna J; Miklerová M
    Cesk Pediatr; 1980 Aug; 35(8):419-22. PubMed ID: 7418077
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. McKusick-Kaufman syndrome: report of the 66th case complicated by a staphyloma of the left eye.
    Cantani A; Santillo C; Cozzi F
    Padiatr Padol; 1991; 26(4):193-6. PubMed ID: 1749628
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of renal tract anomalies by ultrasound.
    Reuss A; Wladimiroff JW; Niermeijer ME
    Prog Clin Biol Res; 1989; 305():13-8. PubMed ID: 2668969
    [No Abstract]   [Full Text] [Related]  

  • 19. Duplication 11 (q21 to 23 leads to qter) syndrome.
    Francke U; Weber F; Sparkes RS; Mattson PD; Mann J
    Birth Defects Orig Artic Ser; 1977; 13(3B):167-86. PubMed ID: 890090
    [No Abstract]   [Full Text] [Related]  

  • 20. [Diagnostic principles for nonchromosomal multiple congenital abnormality syndromes].
    Cherstvoĭ ED; Laziuk GI
    Tsitol Genet; 1979; 13(2):141-3. PubMed ID: 462534
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.