Trisomy recurrence: a reconsideration based on North American data. - Wikidata - awgldk - TriplyDB

Trisomy recurrence: a reconsideration based on North American data.

Trisomy recurrence: a reconsideration based on North American data.

http://www.wikidata.org/entity/Q30943096

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Practice Guidelines for Communicating a Prenatal or Postnatal Diagnosis of Down Syndrome: Recommendations of the National Society of Genetic Counselors Double and multiple chromosomal aneuploidies in spontaneous abortions: A single institutional experience.Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.Cytogenetic and comorbidity profile of Down syndrome in Mansoura University Children's Hospital, Egypt.Mosaic trisomy 18 in a five-month-old infant A Robertsonian Translocation rob (14;15) (q10:q10) in a Patient with Recurrent Abortions: A Case Report.Telomere length and reproductive aging.Mutations of the SYCP3 gene in women with recurrent pregnancy loss.Using FISH to increase the yield and accuracy of karyotypes from spontaneous abortion specimens The importance of rapid aneuploidy screening and prenatal diagnosis in the detection of numerical chromosomal abnormalities.Environmental hazard in the aetiology of somatic and germ cell aneuploidy.Predisposition to aneuploidy in the oocyte.Molecular basis of maternal age-related increase in oocyte aneuploidy.Heterotrisomy recurrence risk: a practical maternal age-dependent approach for excess trisomy 21 risk calculation after a previous autosomal trisomy.Increased susceptibility to maternal aneuploidy demonstrated by comparative genomic hybridization analysis of human MII oocytes and first polar bodies.Why could a woman have three Trisomy 21 pregnancies? - a case report.2006 William Allan Award Address. Having it all.Anencephaly-exencephaly sequence and congenital diaphragmatic hernia in a fetus with 46, XX karyotype: Early prenatal diagnosis, necropsy, and maternal folate pathway genetic analysis.CASP3 protein expression by flow cytometry in Down's syndrome subjects.Preimplantation genetic diagnosis/screening by comprehensive molecular testing.Occurrence of fetal choroid plexus cysts in siblings.Prevalence of Cytogenetic Anomalies in Couples with Recurrent Miscarriages: A Case-control Study.Attitude toward Prenatal Testing and Termination of Pregnancy among Health Professionals and Medical Students in Saudi Arabia.Cytogenetic and epidemiological findings in Down syndrome: England and Wales 1989-2009.Cytological and epidemiological findings in trisomies 13, 18, and 21: England and Wales 2004-2009 Application of chromosomal microarray analysis in products of miscarriage

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P2860

Trisomy recurrence: a reconsideration based on North American data.

http://www.wikidata.org/entity/Q30943096

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2004 nî lūn-bûn

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2004 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2004 թվականի հուլիսին հրատարակված գիտական հոդված

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年學術文章

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name

Trisomy recurrence: a reconsideration based on North American data.

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Trisomy recurrence: a reconsideration based on North American data.

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type

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Trisomy recurrence: a reconsideration based on North American data.

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Trisomy recurrence: a reconsideration based on North American data.

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Trisomy recurrence: a reconsideration based on North American data.

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Trisomy recurrence: a reconsideration based on North American data.

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American Journal of Human Genetics

P1476

Trisomy recurrence: a reconsideration based on North American data.

@en

P2093

Bruce Levin

http://www.w3.org/2001/XMLSchema#string

Dorothy Warburton

http://www.w3.org/2001/XMLSchema#string

Jennie Kline

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Lori Ross

http://www.w3.org/2001/XMLSchema#string

Louis Dallaire

http://www.w3.org/2001/XMLSchema#string

Maya Thangavelu

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P2860

Bisphenol a exposure causes meiotic aneuploidy in the female mouse

To err (meiotically) is human: the genesis of human aneuploidy

Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line.

Chromosomal non-disjunction in human oocytes: is there a mitochondrial connection?

Trisomic pregnancy and earlier age at menopause

Meiotic cohesion requires accumulation of ORD on chromosomes before condensation.

Genetic variation in rates of nondisjunction: association of two naturally occurring polymorphisms in the chromokinesin nod with increased rates of nondisjunction in Drosophila melanogaster

DNA polymorphism analysis in families with recurrence of free trisomy 21.

Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions.

Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies.

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10.1086/423331

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3

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75

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8461435

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15248154

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1182017

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