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 *

161 related articles for article (PubMed ID: 3386650)

  • 1. [Abnormalities-retardation syndrome caused by incomplete triploidy].
    Meinecke P; Engelbrecht R
    Monatsschr Kinderheilkd; 1988 Apr; 136(4):206-9. PubMed ID: 3386650
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Triploidy syndrome and diploid/triploid mixoploidy syndrome].
    Kato R
    Ryoikibetsu Shokogun Shirizu; 2000; (30 Pt 5):361-2. PubMed ID: 11057261
    [No Abstract]   [Full Text] [Related]  

  • 3. Diploid-triploid mixoploidy: clinical and cytogenetic aspects.
    Graham JM; Hoehn H; Lin MS; Smith DW
    Pediatrics; 1981 Jul; 68(1):23-8. PubMed ID: 6264378
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P; Adkins WN; Caspar H; Dumars KW; Gebauer J; Gilbert EF; Grimm T; Habedank M; Hansmann I; Herrmann J; Kaveggia EG; Langenbeck U; Meisner LF; Najafzadeh TM; Opitz JM; Palmer CG; Peters HH; Scholz W; Tavares AS; Wiedeking C
    Am J Med Genet; 1981; 10(2):159-77. PubMed ID: 7315873
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Triploidy in newborn infants].
    Küster W; Beckmann H; Gebauer HJ; Majewski F
    Monatsschr Kinderheilkd; 1988 Apr; 136(4):210-3. PubMed ID: 2838747
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A patient with ring chromosome 13].
    Hammond A; Bijlsma JB
    Ned Tijdschr Geneeskd; 1981 May; 125(19):752-5. PubMed ID: 7242723
    [No Abstract]   [Full Text] [Related]  

  • 7. [Triploidy syndrome: a case report].
    Garzena E; Farinasso D; Prandi GM; Vardeu P; Bagna R; Cavo L; Rinaldi M; Fabris C
    Minerva Pediatr; 1995; 47(7-8):307-11. PubMed ID: 7476758
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interstitial deletion of (17)(p11.2). A microdeletion syndrome. Another example.
    de Almeida JC; Reis DF; Martins RR
    Ann Genet; 1989; 32(3):184-6. PubMed ID: 2817780
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE; Engelen JJ; Schrander-Stumpel CT; Govaerts LC; de Vries B; Vles JS; Wagemans A; Schijns-Fleuren S; Gillessen-Kaesbach G; Fryns JP
    Am J Med Genet; 1995 Nov; 59(3):369-74. PubMed ID: 8599364
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Zimmermann-Laband syndrome in a patient with severe mental retardation.
    Van Buggenhout GJ; Brunner HG; Trommelen JC; Hamel BC
    Genet Couns; 1995; 6(4):321-7. PubMed ID: 8775419
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. Autosomal recessive mode of inheritance of a Coffin-Siris like syndrome.
    Bonioli E; Palmieri A; Bertola A; Bellini C
    Genet Couns; 1995; 6(4):309-12. PubMed ID: 8775417
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pentasomy X: report of patient and studies of X-inactivation.
    Funderburk SJ; Valente M; Klisak I
    Am J Med Genet; 1981; 8(1):27-33. PubMed ID: 7246603
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytogenetic studies in patients with multiple anomalies with or without mental retardation.
    Berry R; Smith AC; McGavran L; O'Hanlon K
    Birth Defects Orig Artic Ser; 1987; 23(6):100-10. PubMed ID: 3435749
    [No Abstract]   [Full Text] [Related]  

  • 15. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q.
    Koiffmann CP; Gonzalez CH; Vianna-Morgante AM; Kim CA; Odone-Filho V; Wajntal A
    Am J Med Genet; 1995 Jul; 58(1):46-9. PubMed ID: 7573155
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML; Punnett HH; Thovichit S; DiGeorge AM; Weiss L
    Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
    [No Abstract]   [Full Text] [Related]  

  • 17. A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiency.
    Hurst JA; Baraitser M; Winter RM
    Am J Med Genet; 1987 Dec; 28(4):965-70. PubMed ID: 3688035
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
    Migliori MV; Cherubini V; Bartolotta E; Pettinari A; Pecora R
    Am J Med Genet; 1994 Jan; 49(1):108-10. PubMed ID: 8172236
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The clinical picture of 13q22-qter duplication in a 2-year-old boy].
    Halasová E; Lukácová M; Bergendiová E; Kamenická E
    Cesk Pediatr; 1987 Aug; 42(8):477-9. PubMed ID: 3664759
    [No Abstract]   [Full Text] [Related]  

  • 20. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R; Lerer I; Maftzir G; Sheinis M; Cohen MM
    Am J Med Genet; 1982 Jun; 12(2):131-9. PubMed ID: 7102721
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.