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 *

138 related articles for article (PubMed ID: 623063)

  • 1. A patient with a partial deletion of the short arm of chromosome 3.
    Verjaal M; De Nef MB
    Am J Dis Child; 1978 Jan; 132(1):43-5. PubMed ID: 623063
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Deletion of the short arm of chromosome 9. A clinically recognisable entity.
    Fryns JP; Pedersen JC; Duyck H; Fabry G; Van den Berghe H
    Eur J Pediatr; 1980 Sep; 134(3):201-4. PubMed ID: 7428770
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Partial monosomy of long arm of chromosome 4 due to interstitial deletion.
    McDermott A; Cain R; Howell R
    Hum Genet; 1980; 53(3):305-7. PubMed ID: 7372333
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A second patient with partial deletion of the short arm of chromosome 3: karyotype 46,XY,del(3)(p25).
    Higginbottom MC; Mascarello JT; Hassin H; McCord WK
    J Med Genet; 1982 Feb; 19(1):71-3. PubMed ID: 7069751
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial deletion of the short arm of chromosome 3.
    Merrild U; Berggreen S; Hansen L; Mikkelsen M; Henningsen K
    Eur J Pediatr; 1981 May; 136(2):211-6. PubMed ID: 7227394
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Terminal long-arm deletion of chromosome 1 in a male infant.
    Dignan PS; Soukup S
    Hum Genet; 1979 Apr; 48(2):151-6. PubMed ID: 457139
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Trigonocephaly and the Opitz C syndrome.
    Sargent C; Burn J; Baraitser M; Pembrey ME
    J Med Genet; 1985 Feb; 22(1):39-45. PubMed ID: 3981579
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Terminal deletion of (1)(q42) and its phenotypical manifestations.
    Andrle M; Erlach A; Mayr WR; Rett A
    Hum Genet; 1978 Feb; 41(1):115-20. PubMed ID: 631857
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Additional case of de novo interstitial deletion del(17)(q21.3q23) and expansion of the phenotype.
    Khalifa MM; MacLeod PM; Duncan AM
    Clin Genet; 1993 Nov; 44(5):258-61. PubMed ID: 7906212
    [TBL] [Abstract][Full Text] [Related]  

  • 10. De novo partial 2q3 trisomy/distal 7p22 monosomy in a malformed newborn with 7p deletion phenotype and craniosynostosis.
    Fryns JP; Haspeslagh M; Agneessens A; van den Berghe H
    Ann Genet; 1985; 28(1):45-8. PubMed ID: 3874588
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletion of the short arm of chromosome 3: a case report with necropsy findings.
    Beneck D; Suhrland MJ; Dicker R; Greco MA; Wolman SR
    J Med Genet; 1984 Aug; 21(4):307-10. PubMed ID: 6492097
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A lethal presentation of de novo deletion 7q.
    McMorrow LE; Toth IR; Gluckson MM; Leff A; Wolman SR
    J Med Genet; 1987 Oct; 24(10):629-31. PubMed ID: 3119853
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Monosomy 1pter.
    Yunis E; Quintero L; Leibovici M
    Hum Genet; 1981; 56(3):279-82. PubMed ID: 7239511
    [No Abstract]   [Full Text] [Related]  

  • 14. Deletion of the short arm of chromosome 20.
    Vianna-Morgante AM; Richieri-Costa A; Rosenberg C
    Clin Genet; 1987 Jun; 31(6):406-9. PubMed ID: 3621644
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Interstitial deletion of the long arm of one 11 chromosome].
    Taillemite JL; Morlier BG; Roux C
    Ann Genet; 1975 Mar; 18(1):61-3. PubMed ID: 1080039
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Interstitial deletion of the long arm of chromosome 3 in a patient with mental retardation and congenital anomalies.
    Franceschini P; Cirillo Silengo M; Davi G; Bianco R; Biagioli M
    Hum Genet; 1983; 64(1):97. PubMed ID: 6873944
    [No Abstract]   [Full Text] [Related]  

  • 17. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20.
    Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H
    Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Duplication-deletion with partial trisomy lq and partial monosomy 3p resulting from a maternal reciprocal translocation rcp (1;3) (q32;p25).
    Schinzel A
    J Med Genet; 1981 Feb; 18(1):64-8. PubMed ID: 7253002
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel deletion on the short arm of chromosome 17 in a patient with multiple cardiac anomalies.
    Kowase K; Nakamura T; Okumura W; Okamoto E; Yamaguchi E; Sato H; Arai M; Imai S; Hasegawa A; Nagai R
    Jpn Circ J; 1997 Oct; 61(10):882-5. PubMed ID: 9387072
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interstitial deletion of the long arm of chromosome 2 (q31q33) in a girl with multiple anomalies and mental retardation.
    Franceschini P; Cirillo Silengo M; Davi G; Bianco R; Biagioli M
    Hum Genet; 1983; 64(1):98. PubMed ID: 6873945
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.