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.
152 related articles for article (PubMed ID: 7286975)
21. Tissue-specific mosaicism among fetuses with prenatally diagnosed diaphragmatic hernia. Donnenfeld AE; Campbell TJ; Byers J; Librizzi RJ; Weiner S Am J Obstet Gynecol; 1993 Oct; 169(4):1017-21. PubMed ID: 8238112 [TBL] [Abstract][Full Text] [Related]
22. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies. Genuardi M; Tozzi C; Pomponi MG; Stagni ML; Della Monica M; Scarano G; Calvieri F; Torrisi L; Neri G Eur J Hum Genet; 1999; 7(4):421-6. PubMed ID: 10352932 [TBL] [Abstract][Full Text] [Related]
23. Chromosomal mosaicism in amniotic cell culture. A diagnostic Dilemma. Kohn G; Mennuti MT; Kaback M; Schwartz RM; Chemke J; Goldman B; Mellman WJ Isr J Med Sci; 1975 May; 11(5):476-81. PubMed ID: 1158661 [TBL] [Abstract][Full Text] [Related]
24. [Rapid detection of the most common chromosomal aneuploidies in the second-trimester amniotic fluid using QF-PCR]. Švecová I; Burjanivová T; Kršiaková J; Lasabová Z; Biringer K; Kapustová I; Móricová P; Danko J Ceska Gynekol; 2013 Aug; 78(4):373-8. PubMed ID: 24040987 [TBL] [Abstract][Full Text] [Related]
25. Prenatal detection of de novo inversion of chromosome 9 with duplicated heterochromatic region and postnatal follow-up. Kim JJ; Rhee HS; Chung YT; Park SY; Choi SK Exp Mol Med; 1999 Sep; 31(3):134-6. PubMed ID: 10551261 [TBL] [Abstract][Full Text] [Related]
26. Balanced and unbalanced pericentric inversion of a chromosome 14. Pfeiffer RA; Kessel E Hum Genet; 1978 Jul; 43(1):103-6. PubMed ID: 669718 [TBL] [Abstract][Full Text] [Related]
27. Prenatal fetal karyotyping and maternal serum alpha-fetoprotein screening. Gosden C; Buckton K; Fotheringham Z; Brock DJ Br Med J (Clin Res Ed); 1981 Jan; 282(6260):255-8. PubMed ID: 6161673 [TBL] [Abstract][Full Text] [Related]
28. Prenatal detection of a pure trisomy 10p case. Gunduz C; Cogulu O; Sagol S; Zekioglu O; Ozkinay C; Ozkinay F Prenat Diagn; 2003 Apr; 23(4):356-8. PubMed ID: 12673647 [No Abstract] [Full Text] [Related]
29. Complex balanced translocation of chromosomes 2, 3, and 13. Muneer RS; Donaldson DL; Rennert OM Hum Genet; 1981; 59(2):182-4. PubMed ID: 7327579 [No Abstract] [Full Text] [Related]
30. Banding resolution of amniotic cell chromosome preparations for prenatal diagnosis. Kao YS; Kao GA; Walters CS Am J Clin Pathol; 1990 Jun; 93(6):765-70. PubMed ID: 2346134 [TBL] [Abstract][Full Text] [Related]
31. Antenatal genetic diagnosis in a kindred with a 15p plus chromosome. Hahnemann N; Eiberg H Clin Genet; 1973 Jun; 4(6):464-73. PubMed ID: 4132613 [No Abstract] [Full Text] [Related]
32. Recombinant chromosome 18 in two offspring of a chromosome 18 inversion heterozygote. Andrews T; Gardiner AC; Boon AR Ann Genet; 1982; 25(3):185-8. PubMed ID: 6982674 [TBL] [Abstract][Full Text] [Related]
33. Decreased levels of amniotic fluid alpha-fetoprotein associated with Down syndrome. Davis RO; Cosper P; Huddleston JF; Bradley EL; Finley SC; Finley WH; Milunsky A Am J Obstet Gynecol; 1985 Nov; 153(5):541-4. PubMed ID: 2414991 [TBL] [Abstract][Full Text] [Related]
34. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome. Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851 [TBL] [Abstract][Full Text] [Related]
36. Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q. Chen CP; Tsai FJ; Lee CC; Chen WL; Pan CW; Wu PC; Wang W Genet Couns; 2010; 21(3):353-7. PubMed ID: 20964129 [No Abstract] [Full Text] [Related]
37. Results and pitfalls in prenatal cytogenetic diagnosis. Hsu LY; Dubin EC; Kerenyi T; Hirschhorn K J Med Genet; 1973 Jun; 10(2):112-9. PubMed ID: 4268389 [TBL] [Abstract][Full Text] [Related]
38. Prenatal detection of D trisomy. Laurence KM; Gregory PJ; Sharp F J Med Genet; 1974 Dec; 11(4):398-400. PubMed ID: 4443990 [TBL] [Abstract][Full Text] [Related]
39. Prenatal diagnosis of inv(X)(q12q28) in a male fetus. Neu RL; Brar HS; Koos BJ J Med Genet; 1988 Jan; 25(1):52-3. PubMed ID: 3351892 [TBL] [Abstract][Full Text] [Related]
40. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion. Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Lee MS; Yang CW; Wang W Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]