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: 1002155)

  • 1. "Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosis.
    Gimelli G; Porro E; Santi F; Scappaticci S; Zuffardi O
    Hum Genet; 1976 Dec; 34(3):315-8. PubMed ID: 1002155
    [TBL] [Abstract][Full Text] [Related]  

  • 2. rDNA and acrocentric chromosomes in man. I. rDNA levels in a subject carrier of a 8p/13p balanced translocation and in his unbalanced son.
    Guanti G; Mollica G; Polimeno L; Maritato F
    Hum Genet; 1976 Jul; 33(2):103-7. PubMed ID: 939562
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homozygosity for a Y/22 chromosome translocation: t(Y;22) (q12;p12/13).
    Leschot NJ; von den Velden J; Marinkovic-Ilsen A; Darling SM; Nijenhuis LE
    Clin Genet; 1986 Mar; 29(3):251-7. PubMed ID: 3698333
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Segregation of a t(14q22q) chromosome in a large kindred.
    Neu RL; Valentine FA; Gardner LI
    Clin Genet; 1975 Jul; 8(1):30-6. PubMed ID: 1149319
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome.
    Dallapiccola B; Bollea G; Mazzilli C; Gandini E
    Hum Genet; 1976 Jul; 33(1):73-6. PubMed ID: 939560
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis and follow up of a child with a complex chromosome rearrangement.
    Bogart MH; Bradshaw CL; Jones OW; Schanberger JE
    J Med Genet; 1986 Apr; 23(2):180-3. PubMed ID: 3712398
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Multiple chromosome aberrations in 3 generations of a family and Down's syndrome resulting from partial trisomy of chromosome 21 (q21--q22)].
    Butomo IV; Prozorova MV; Khitrikova LE
    Tsitol Genet; 1984; 18(3):223-8. PubMed ID: 6235655
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Prenatal detection of crying cat syndrome due to balanced translocation in one parent].
    Barjaktarović N; Pendić B; Garzicić B; Popovic M; Paljm A
    Nouv Presse Med; 1977 Jan; 6(3):180-2. PubMed ID: 834552
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Translocation (13q21q). Four generation family study with analysis of satellite associations, fluorescent markers, and prenatal diagnosis.
    Mikkelsen M; Hansson A; Jacobsen P; Hobolth N
    Humangenetik; 1975; 27(4):303-7. PubMed ID: 125223
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
    Chen CP; Chern SR; Wu PC; Tsai FJ; Lee CC; Town DD; Chen WL; Chen LF; Lee MS; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2009 Dec; 48(4):389-99. PubMed ID: 20045761
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring.
    Lindenbaum RH; Bobrow M
    J Med Genet; 1975 Mar; 12(1):29-43. PubMed ID: 123589
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mating between two balanced translocation carriers in two unrelated families.
    Dallapiccola B; Chessa L; Brinchi V; Frontali M; Gandini E
    Hum Genet; 1983; 65(2):165-8. PubMed ID: 6654331
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Meiotic and sperm aneuploidy studies in three carriers of Robertsonian translocations and small supernumerary marker chromosomes.
    Kirkpatrick G; Ren H; Liehr T; Chow V; Ma S
    Fertil Steril; 2015 May; 103(5):1162-9.e7. PubMed ID: 25796321
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Father and daughter with presumptive isochromosome satellites-short arms D or G.
    Nielsen J; Hreidarsson AB
    Humangenetik; 1973 Sep; 19(3):271-4. PubMed ID: 4763931
    [No Abstract]   [Full Text] [Related]  

  • 15. Two balanced translocations in three generations of a pedigree: t(7;10) (q11;q22) and t(14;21) (14qter to cen to 21qter)1.
    Bass HN; Sparkes RS
    J Med Genet; 1979 Jun; 16(3):215-8. PubMed ID: 157395
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A familial extra small marker autosome in persons with normal phenotype.
    Fried K; Rosenblatt M
    Hum Hered; 1979; 29(6):371-3. PubMed ID: 511193
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Balanced reciprocal translocation at amniocentesis: cytogenetic detection and implications for genetic counseling.
    Zhang HG; Zhang XY; Zhang HY; Tian T; Xu SB; Liu RZ
    Genet Mol Res; 2016 Aug; 15(3):. PubMed ID: 27706592
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation].
    Liu JY; Wang XR; Zeng XL; Zhang CS; Song YC
    Yi Chuan Xue Bao; 2004 Feb; 31(2):125-31. PubMed ID: 15473301
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Large translocation t(3q-;4p+) as probable cause for semisterility.
    Sarto G; Therman E
    Fertil Steril; 1976 Jul; 27(7):784-8. PubMed ID: 985759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12).
    Howard-Peebles PN; Yarbrough KM; Stoddard GR; Rary JM
    Clin Genet; 1977 Jan; 11(1):46-52. PubMed ID: 830449
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.