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 *

99 related articles for article (PubMed ID: 1563090)

  • 21. Unusual chromosome 9 variant with an extra G-dark and C-negative segment in the short arm, proximal to the centromere: a case study.
    Chen PY; Wu HM; Kuo PL; Tzeng CC
    Zhonghua Yi Xue Za Zhi (Taipei); 1999 Feb; 62(2):121-4. PubMed ID: 10063724
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Variants of chromosome 9 with additional euchromatic bands: two case reports.
    Reddy KS
    Am J Med Genet; 1996 Sep; 64(4):536-8. PubMed ID: 8870918
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Neural tube defects].
    Maximilian C
    Pediatr Pol; 1972; 21(6):557-9. PubMed ID: 4573805
    [No Abstract]   [Full Text] [Related]  

  • 24. Prenatal diagnosis of a large heteromorphic region in a chromosome 5: implications for genetic counseling.
    Fineman RM; Issa B; Weinblatt V
    Am J Med Genet; 1989 Apr; 32(4):498-9. PubMed ID: 2773992
    [TBL] [Abstract][Full Text] [Related]  

  • 25. An unusual G-negative band within 1qh region a rare variant or an abnormality?
    Verma RS; Kleyman SM; Conte RA
    Ann Genet; 1997; 40(4):229-31. PubMed ID: 9526619
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Extra band in the 9qh+ chromosome in a normal father and in his child with multiple congenital anomalies.
    Silengo MC; Davi GF; Franceschini P
    Hum Genet; 1982; 60(3):294. PubMed ID: 7106764
    [No Abstract]   [Full Text] [Related]  

  • 27. Distal 15q trisomy with Dandy-Walker malformation in a female infant.
    Ieshima A; Takeshita K; Shirasaka Y; Nakao Y; Kisa T
    Jinrui Idengaku Zasshi; 1985 Sep; 30(3):227-32. PubMed ID: 3834203
    [No Abstract]   [Full Text] [Related]  

  • 28. Non C-banding variants in some normal families might be homogeneously staining regions.
    Webb GC; Krumins EJ; Eichenbaum SZ; Voullaire LE; Earle E; Choó KH
    Hum Genet; 1989 Apr; 82(1):59-62. PubMed ID: 2714780
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Molecular cytogenetic studies of duplication 9q32-->q34.3 inserted into 9q13.
    Hou JW; Wang TR
    Clin Genet; 1995 Sep; 48(3):148-50. PubMed ID: 8556822
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Unusual chromosome 9 polymorphism and reproductive failure.
    Fryns JP; Kleczkowska A; Londers L; van den Berghe H
    Ann Genet; 1985; 28(1):49-51. PubMed ID: 3874589
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A rare heterochromatic variant of chromosome 4.
    Docherty Z; Bowser-Riley SM
    J Med Genet; 1984 Dec; 21(6):470-2. PubMed ID: 6512840
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Major malformation syndrome and apparently balanced chromosomal abnormality: holoprosencephaly and 5p; 12q translocation].
    Cousin J; Creusy C; Croquette MF; Vittu G
    J Genet Hum; 1988 Jan; 36(1-2):83-8. PubMed ID: 3288708
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The role of genetics in understanding hydrocephalus and spina bifida. An update.
    Jouet M
    Eur J Pediatr Surg; 1996 Dec; 6 Suppl 1():35-6. PubMed ID: 9008819
    [No Abstract]   [Full Text] [Related]  

  • 34. Molecular cytogenetic characterization of two types of chromosome 9 variants.
    Wang JC; Miller WA
    Cytogenet Cell Genet; 1994; 67(3):190-2. PubMed ID: 8062595
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Anencephaly.
    Lorber J
    Clin Pediatr (Phila); 1971 Jan; 10(1):3-4. PubMed ID: 4925833
    [No Abstract]   [Full Text] [Related]  

  • 36. A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility.
    Cai T; Yu P; Tagle DA; Lu D; Chen Y; Xia J
    Hum Reprod; 2001 Jan; 16(1):59-62. PubMed ID: 11139537
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus).
    Wright YM; Clark WE; Breg WR
    J Med Genet; 1974 Mar; 11(1):69-75. PubMed ID: 4134620
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Patients with deletions of 9q22q34 do not define a syndrome: three case reports and a literature review.
    Farrell SA; Siegel-Bartelt J; Teshima I
    Clin Genet; 1991 Sep; 40(3):207-14. PubMed ID: 1773536
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Eugenic counseling after a birth of an infant with congenital malformations].
    Beolchini PE
    Minerva Med; 1972 Nov; 63(85):4660-4. PubMed ID: 4264406
    [No Abstract]   [Full Text] [Related]  

  • 40. Rare variants of chromosome 9 with extra G positive band within the qh region are not alike.
    Conte RA; Gupta S; Brennan JP; Verma RS
    J Med Genet; 1995 May; 32(5):405-6. PubMed ID: 7542346
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.