Avoiding a second amniocentesis to corroborate prenatal diagnosis by using refrigerated samples.

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Avoiding a second amniocentesis to corroborate prenatal diagnosis by using refrigerated samples.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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Avoiding a second amniocentesi ...... by using refrigerated samples.

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Avoiding a second amniocentesi ...... by using refrigerated samples.

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Avoiding a second amniocentesi ...... by using refrigerated samples.

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Avoiding a second amniocentesi ...... by using refrigerated samples.

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Avoiding a second amniocentesi ...... by using refrigerated samples.

@en

Avoiding a second amniocentesi ...... by using refrigerated samples.

@nl

P1476

Avoiding a second amniocentesi ...... by using refrigerated samples

@en

P2093

A Barrios-Martinez

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E Cuétara

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E Morales

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G Huertas-Perez

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M Garcia

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O Molina-Gamboa

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U Suarez-Mayedo

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P2860

Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies.

French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature.

The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.

Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells.

Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly.

Unexplained autism is frequently associated with low-level mosaic aneuploidy.

Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony.

Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.

Misinterpretation of trisomy 18 as a pseudomosaicism at third-trimester amniocentesis of a child with a mosaic 46,XY/47,XY, +3/48,XXY, +18 karyotype.

A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes.

P304

839-843

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scholarly article

P356

10.1080/14767058.2016.1188380

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P433

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P478

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P50

Luis A Méndez-Rosado

P577

2016-05-26T00:00:00Z

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P698

27160879

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P921

amniocentesis