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Items: 1 to 20 of 26

1.

From karyotyping to array-CGH in prenatal diagnosis.

Lichtenbelt KD, Knoers NV, Schuring-Blom GH.

Cytogenet Genome Res. 2011;135(3-4):241-50. doi: 10.1159/000334065. Review.

PMID:
22086062
2.

ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis.

[No authors listed]

Obstet Gynecol. 2009 Nov;114(5):1161-3. doi: 10.1097/AOG.0b013e3181c33cad.

PMID:
20168129
3.

Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH.

Ballif BC, Hornor SA, Sulpizio SG, Lloyd RM, Minier SL, Rorem EA, Theisen A, Bejjani BA, Shaffer LG.

Genet Med. 2007 Mar;9(3):150-62.

PMID:
17413419
4.

Array painting using microdissected chromosomes to map chromosomal breakpoints.

Backx L, Van Esch H, Melotte C, Kosyakova N, Starke H, Frijns JP, Liehr T, Vermeesch JR.

Cytogenet Genome Res. 2007;116(3):158-66.

PMID:
17317954
5.

A comprehensive analysis of common copy-number variations in the human genome.

Wong KK, deLeeuw RJ, Dosanjh NS, Kimm LR, Cheng Z, Horsman DE, MacAulay C, Ng RT, Brown CJ, Eichler EE, Lam WL.

Am J Hum Genet. 2007 Jan;80(1):91-104.

6.

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.

Ballif BC, Rorem EA, Sundin K, Lincicum M, Gaskin S, Coppinger J, Kashork CD, Shaffer LG, Bejjani BA.

Am J Med Genet A. 2006 Dec 15;140(24):2757-67.

PMID:
17103431
7.

Supernumerary marker chromosomes detected in 100,000 prenatal diagnoses: molecular cytogenetic studies and clinical significance.

Huang B, Solomon S, Thangavelu M, Peters K, Bhatt S.

Prenat Diagn. 2006 Dec;26(12):1142-50.

PMID:
17009345
8.

Identification, characterization and clinical implications of two markers detected at prenatal diagnosis.

Leite RP, Souto M, Carvalho B, Martins M, Chaves R, Morais A, Guedes-Pinto H, Wienberg J, Ribeiro E.

Prenat Diagn. 2006 Oct;26(10):920-4.

PMID:
16845683
9.

Prenatal identification of small supernumerary marker chromosomes by FISH in an infant born with mild congenital anomalies.

Chen M, Chang SP, Yin PL, Sapeta M, Barringer S, Kuo SJ, Yu HT, Wang BB.

Prenat Diagn. 2006 Apr;26(4):383-7. No abstract available.

PMID:
16566043
10.

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.

Liehr T, Starke H, Senger G, Melotte C, Weise A, Vermeesch JR.

Am J Med Genet A. 2006 Jan 1;140(1):46-51. Review.

PMID:
16333826
11.

Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.

Liehr T, Mrasek K, Weise A, Dufke A, Rodríguez L, Martínez Guardia N, Sanchís A, Vermeesch JR, Ramel C, Polityko A, Haas OA, Anderson J, Claussen U, von Eggeling F, Starke H.

Cytogenet Genome Res. 2006;112(1-2):23-34.

PMID:
16276087
12.

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.

13.

Prenatal diagnosis of minute supernumerary marker chromosomes.

Cotter PD, Drexler K, Corley AL, Covert SM, Moland JS, Govberg IJ, Norton ME.

Gynecol Obstet Invest. 2005;60(1):27-38.

PMID:
15689640
14.

Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.

Starke H, Nietzel A, Weise A, Heller A, Mrasek K, Belitz B, Kelbova C, Volleth M, Albrecht B, Mitulla B, Trappe R, Bartels I, Adolph S, Dufke A, Singer S, Stumm M, Wegner RD, Seidel J, Schmidt A, Kuechler A, Schreyer I, Claussen U, von Eggeling F, Liehr T.

Hum Genet. 2003 Dec;114(1):51-67.

PMID:
13680362
15.

Additional patient with del(12)(q21.2q22): further evidence for a candidate region for cardio-facio-cutaneous syndrome?

Rauen KA, Albertson DG, Pinkel D, Cotter PD.

Am J Med Genet. 2002 Jun 1;110(1):51-6.

PMID:
12116271
16.

Assembly of microarrays for genome-wide measurement of DNA copy number.

Snijders AM, Nowak N, Segraves R, Blackwood S, Brown N, Conroy J, Hamilton G, Hindle AK, Huey B, Kimura K, Law S, Myambo K, Palmer J, Ylstra B, Yue JP, Gray JW, Jain AN, Pinkel D, Albertson DG.

Nat Genet. 2001 Nov;29(3):263-4.

PMID:
11687795
17.

Prenatal detection of extra structurally abnormal chromosomes (ESACs): new cases and a review of the literature.

Hastings RJ, Nisbet DL, Waters K, Spencer T, Chitty LS.

Prenat Diagn. 1999 May;19(5):436-45. Review.

PMID:
10360512
19.
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