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 *

89 related articles for article (PubMed ID: 3842997)

  • 1. [Prenatal cytogenetic diagnosis of a 69,XXX/46,XX fetus].
    Doria Lamba Carbone L; Pierluigi M; Ferro MA
    Pathologica; 1985; 77(1052):761-6. PubMed ID: 3842997
    [No Abstract]   [Full Text] [Related]  

  • 2. Parental decisions following prenatal diagnosis of sex chromosome aneuploidy: a trend over time.
    Christian SM; Koehn D; Pillay R; MacDougall A; Wilson RD
    Prenat Diagn; 2000 Jan; 20(1):37-40. PubMed ID: 10701849
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Antenatal diagnosis of an XXX female. A dilemma for genetic counseling.
    Krone LR; Prichard LL; Bradshaw CL; Jones OW; Peterson RM; Dixson BK
    West J Med; 1975 Jul; 123(1):17-21. PubMed ID: 1154778
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ascertainment of 68,XX double aneuploidy by midtrimester biochemical screening: a case report.
    Ross EL; Bofill JA; Shenefelt RE; Yu CW; Perry KG
    Am J Perinatol; 1998 Apr; 15(4):229-32. PubMed ID: 9565219
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The problem of sex chromosome aneuploidy in genetic counseling using amniocentesis].
    Engel E; Engel-De Montmollin M; Delozier C
    J Genet Hum; 1980 Sep; 28(3):257-66. PubMed ID: 7463026
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal diagnosis and management of sex chromosome aneuploidy: a report on 98 cases.
    Brun JL; Gangbo F; Wen ZQ; Galant K; Taine L; Maugey-Laulom B; Roux D; Mangione R; Horovitz J; Saura R
    Prenat Diagn; 2004 Mar; 24(3):213-8. PubMed ID: 15057956
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Unexpected chromosomal abnormalities in prenatal diagnosis. 4 case reports with preservation of the pregnancy].
    Gilgenkrantz S; Schweitzer M; Droulle P; Mujica P; Lerond MA; Boué J
    J Genet Hum; 1986 Aug; 34(3-4):245-54. PubMed ID: 3760829
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Decisions following the intrauterine diagnosis of sex chromosome aneuploidy.
    Robinson A; Bender BG; Linden MG
    Am J Med Genet; 1989 Dec; 34(4):552-4. PubMed ID: 2624268
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal/heterosomal mixoploids: a report on two patients, a female with a 45, Z/47,XX plus 21 and a male with A 45,X/47,XY, plus 21 chromosome constitution.
    Hustinx TW; Haar BG; Scheres JM; Rutten FJ
    Ann Genet; 1974 Dec; 17(4):225-34. PubMed ID: 4281287
    [No Abstract]   [Full Text] [Related]  

  • 10. Investigation of acephalus.
    Deacon JS; Machin GA; Martin JM; Nicholson S; Nwankwo DC; Wintemute R
    Am J Med Genet; 1980; 5(1):85-99. PubMed ID: 7190356
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Paucity of 47,XXX and 46,XX/47,XXX among routine diagnostic cytogenetic referrals.
    Bell J; Pearn J
    Med J Aust; 1983 Nov; 2(11):535-6. PubMed ID: 6633377
    [No Abstract]   [Full Text] [Related]  

  • 12. [Prenatal diagnosis of hereditary diseases using chorionic villi].
    Rumenić-Garzicić L; Krajinović M
    Jugosl Ginekol Perinatol; 1985; 25(1-2):25-8. PubMed ID: 4087929
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Karyotype 49, XXXXY in an infant].
    Serville F; Guillard JM; de Joigny C; Cixous P; Fontan D; Ruffié M; Verger P
    Pediatrie; 1973; 28(1):83-90. PubMed ID: 4715469
    [No Abstract]   [Full Text] [Related]  

  • 14. Prenatal diagnosis of a fetus with partial trisomy 7p.
    Ozgun MT; Batukan C; Basbug M; Akgun H; Caglayan O; Dundar M
    Fetal Diagn Ther; 2007; 22(3):229-32. PubMed ID: 17228165
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidy.
    Mezei G; Papp C; Tóth-Pál E; Beke A; Papp Z
    Obstet Gynecol; 2004 Jul; 104(1):94-101. PubMed ID: 15229006
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of 45, X/46, XY.
    Waurin JL; Adams JE; Baramki TA
    Md Med J; 1985 Sep; 34(9):883-4. PubMed ID: 3851135
    [No Abstract]   [Full Text] [Related]  

  • 17. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases].
    Zhao L; Li H; Xue YQ; Pan JL; Wu YF; Lu M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):611-4. PubMed ID: 15583994
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Forty-two supernumerary marker chromosomes (SMCs) in 43,273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies.
    Bartsch O; Loitzsch A; Kozlowski P; Mazauric ML; Hickmann G
    Eur J Hum Genet; 2005 Nov; 13(11):1192-204. PubMed ID: 16077735
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Full karyotyping, rapid aneuploidy diagnosis or both when invasive prenatal testing is performed for diagnosis of thalassaemia?
    Tse KY; Leung WC; Leung KY; Lee CP; Ng LK; Lau ET; Chan V; Tang MH
    Mol Hum Reprod; 2006 Jan; 12(1):55-9. PubMed ID: 16421217
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The practicing physician facing current problems in genetics].
    Juillard E; Grosset L
    Rev Med Suisse Romande; 1973 Sep; 93(9):655-68. PubMed ID: 4272167
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.