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Items: 1 to 20 of 455

1.

Trisomy 13 mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy.

Chen M, Yeh GP, Shih JC, Wang BT.

Prenat Diagn. 2004 Feb;24(2):137-43. Review.

PMID:
14974123
2.

Prenatal diagnosis of trisomy 3 mosaicism.

Zaslav AL, Pierno G, Davis J, Fougner A, Jacob J, Kazi R, Blumenthal D, Sturim S, Shaham M, Fox J.

Prenat Diagn. 2004 Sep;24(9):693-6. Review.

PMID:
15386452
3.

Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.

Chen CP, Chern SR, Lee CC, Chang TY, Wang W, Tzen CY.

Prenat Diagn. 2004 Jan;24(1):38-44. Review.

PMID:
14755408
4.

Maternal uniparental disomy for chromosome 22 in a child with generalized mosaicism for trisomy 22.

de Pater JM, Schuring-Blom GH, van den Bogaard R, van der Sijs-Bos CJ, Christiaens GC, Stoutenbeek P, Leschot NJ.

Prenat Diagn. 1997 Jan;17(1):81-6.

PMID:
9021833
5.

Rare trisomy mosaicism diagnosed in amniocytes, involving an autosome other than chromosomes 13, 18, 20, and 21: karyotype/phenotype correlations.

Hsu LY, Yu MT, Neu RL, Van Dyke DL, Benn PA, Bradshaw CL, Shaffer LG, Higgins RR, Khodr GS, Morton CC, Wang H, Brothman AR, Chadwick D, Disteche CM, Jenkins LS, Kalousek DK, Pantzar TJ, Wyatt P.

Prenat Diagn. 1997 Mar;17(3):201-42.

PMID:
9110367
6.

Trisomy 12/monosomy X/normal female mosaicism: prenatal detection and confirmation in a liveborn.

Spiro R, Rita D, Jazmines L, Jones C, Booth CW.

Prenat Diagn. 1996 Aug;16(8):734-40.

PMID:
8878284
7.

Dilemma of trisomy 20 mosaicism detected prenatally: is it an innocent finding?

Reish O, Wolach B, Amiel A, Kedar I, Dolfin T, Fejgin M.

Am J Med Genet. 1998 Apr 28;77(1):72-5. Review.

PMID:
9557898
8.

Prenatal diagnosis of trisomy 4 mosaicism.

Zaslav AL, Blumenthal D, Willner JP, Pierno G, Jacob J, Fox JE.

Am J Med Genet. 2000 Dec 11;95(4):381-4. Review.

PMID:
11186894
9.

Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development.

Baty BJ, Olson SB, Magenis RE, Carey JC.

Am J Med Genet. 2001 Mar 15;99(3):210-6. Review.

PMID:
11241492
10.

Clinical outcome and follow-up of the first reported case of Russell-Silver syndrome with the unique combination of maternal uniparental heterodisomy 7 and mosaic trisomy 7.

Font-Montgomery E, Stone KM, Weaver DD, Vance GH, Das S, Thurston VC.

Birth Defects Res A Clin Mol Teratol. 2005 Aug;73(8):577-82.

PMID:
16007591
11.

Management of prenatally detected trisomy 8 mosaicism.

van Haelst MM, Van Opstal D, Lindhout D, Los FJ.

Prenat Diagn. 2001 Dec;21(12):1075-8.

PMID:
11746167
12.

Trisomy 16 and trisomy 16 Mosaicism: a review.

Benn P.

Am J Med Genet. 1998 Sep 1;79(2):121-33. Review.

PMID:
9741470
13.

Trisomy 20 mosaicism and nonmosaic trisomy 20: a report of 2 cases.

Joó JG, Beke A, Tóth-Pál E, Hargitai B, Szigeti Z, Papp C, Papp Z.

J Reprod Med. 2006 Mar;51(3):209-12.

PMID:
16674019
14.

Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.

Habecker-Green JG, Naeem R, Gold H, O'Grady JP, Kanaan C, Bayer-Zwirello L, Murray MS, Cohn GM.

J Perinatol. 1998 Sep-Oct;18(5):395-8.

PMID:
9766419
15.

Prenatal diagnosis of mosaic trisomy 13: a case report.

Eubanks SR, Kuller JA, Amjadi D, Powell CM.

Prenat Diagn. 1998 Sep;18(9):971-4.

PMID:
9793984
16.

True trisomy 2 mosaicism in amniocytes and newborn liver associated with multiple system abnormalities.

Sago H, Chen E, Conte WJ, Cox VA, Goldberg JD, Lebo RV, Golabi M.

Am J Med Genet. 1997 Oct 31;72(3):343-6. Review.

PMID:
9332667
17.

Prenatal diagnosis of trisomy 12 mosaicism: physical and developmental follow-up.

Meck JM, Kozma C, Tchabo JG, King JC, Lencki S, Pinckert TL.

Prenat Diagn. 1994 Sep;14(9):878-83.

PMID:
7845898
19.

Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotype.

Wieczorek D, Prott EC, Robinson WP, Passarge E, Gillessen-Kaesbach G.

Prenat Diagn. 2003 Feb;23(2):128-33.

PMID:
12575019
20.

Pre- and postnatal findings in trisomy 17 mosaicism.

Utermann B, Riegel M, Leistritz D, Karall T, Wisser J, Meisner L, Fauth C, Baldinger R, Johnson J, Erdel M, Taralczak M, Pauli RM, Baumer A, Schinzel A, Kotzot D.

Am J Med Genet A. 2006 Aug 1;140(15):1628-36.

PMID:
16802327

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