(Q33763597)

29 July 2017

title

On the paternal origin of trisomy 21 Down syndrome (English)

1 reference

29 July 2017

1 reference

Maj A Hultén

1

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29 July 2017

Suketu D Patel

2

1 reference

29 July 2017

Magnus Westgren

3

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29 July 2017

Nikos Papadogiannakis

4

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29 July 2017

Anna Maria Jonsson

5

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29 July 2017

Jon Jonasson

6

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29 July 2017

Erik Iwarsson

7

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29 July 2017

publication date

23 February 2010

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29 July 2017

published in

Molecular Cytogenetics

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29 July 2017

volume

3

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29 July 2017

page(s)

4

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Genetics. Genetic control of hotspots.

29 July 2017

cites work

1 reference

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Maternal age and chromosomally abnormal pregnancies: what we know and what we wish we knew

22 June 2018

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Meiotic recombination in human oocytes.

22 June 2018

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Broad-scale recombination patterns underlying proper disjunction in humans

22 June 2018

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On the origin of the maternal age effect in trisomy 21 Down syndrome: the Oocyte Mosaicism Selection model

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

The complex relationship between folate/homocysteine metabolism and risk of Down syndrome

22 June 2018

1 reference

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Clinical practice. Prenatal screening for aneuploidy

22 June 2018

1 reference

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Germ cell sex determination in mammals

22 June 2018

1 reference

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Telomeres and reproductive aging

22 June 2018

1 reference

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Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Maternal origin of the human aneuploidies. Are homolog synapsis and recombination to blame? Notes (learned) from the underbelly.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

On the origin of trisomy 21 Down syndrome

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Faulty spindle checkpoint and cohesion protein activities predispose oocytes to premature chromosome separation and aneuploidy

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Complex and segmental uniparental disomy updated

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Meiotic errors in human oogenesis and spermatogenesis

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

New insights into human nondisjunction of chromosome 21 in oocytes

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Human female meiosis: what makes a good egg go bad?

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Spindle formation, chromosome segregation and the spindle checkpoint in mammalian oocytes and susceptibility to meiotic error

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Meiosis in oocytes: predisposition to aneuploidy and its increased incidence with age.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Sexual dimorphism of gonadal development

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Aneuploidy and confined chromosomal mosaicism in the developing human brain.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Fertility in men with Down syndrome: a case report

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

A fascination with chromosome rescue in uniparental disomy: Mendelian recessive outlaws and imprinting copyrights infringements

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Migration of human and mouse primordial germ cells and colonization of the developing ovary: an ultrastructural and cytochemical study

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Mongolism; a chromosomal disease (trisomy).

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Stable variants of sperm aneuploidy among healthy men show associations between germinal and somatic aneuploidy.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Female predominance (low sex ratio) in 47,+21 mosaics

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Chromosome 21 disomy in the spermatozoa of the fathers of children with trisomy 21, in a population with a high prevalence of Down syndrome: increased incidence in cases of paternal origin.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Sex ratios in fetuses and liveborn infants with autosomal aneuploidy.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down Syndrome Cytogenetic Register and the Association of Clinical Cytogeneticists

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Dermatoglyphic studies in the parents of trisomy 21 children I. Distribution of dermatoglyphic discriminants.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Dermatoglyphic peculiarities in Down's syndrome detection of mosaicism and balanced translocation carriers.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Maternal-age effect in aneuploidy: does altered embryonic selection play a role?

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Parental dermatoglyphics in Down's syndrome. A ten-year study

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Paternal trisomy 21 mosaicism and Down's anomaly.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Paternal trisomy 21 mosaicism and Down's syndrome

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Mosaic Down's syndrome in a father and daughter

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

A direct cytogenetic technique for assessing the rate of first meiotic non-disjunction in the human male by the analysis of cells at metaphase II.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Fertility in a male with trisomy 21

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Reproduction in Down's syndrome

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

The chromosome complement of human gametes

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

DNA polymorphism analysis in families with recurrence of free trisomy 21

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Trisomy 21 mosaicism in two subjects from two generations

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Mosaicism-trisomy in fathers of two children with Down's syndrome

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Susceptibility to aneuploidy in young mothers of Down syndrome children.

22 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Chromosome instability is common in human cleavage-stage embryos.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Preimplantation aneuploid embryos undergo self-correction in correlation with their developmental potential.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Commentary: Clustering in Down syndrome

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

The association of folate, zinc and antioxidant intake with sperm aneuploidy in healthy non-smoking men.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Rescuing distal crossovers.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Individual variation in the frequency of sperm aneuploidy in humans.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Number of germ cells and somatic cells in human fetal ovaries during the first weeks after sex differentiation.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Mitotic errors in chromosome 21 of human preimplantation embryos are associated with non-viability.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Relationship between genetic anomalies of different levels and deviations in dermatoglyphic traits. Part 4: Dermatoglyphic peculiarities of males and females with Down syndrome. Family study.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Recurrence risks for trisomies 13, 18, and 21

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Spatial expression of germ cell markers during maturation of human fetal male gonads: an immunohistochemical study

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2848052

Trisomy 21 mosaicism in gonads with unexpectedly high recurrence risks

30 October 2018

1 reference

12 December 2020

Observations on mosaic parents of mongol propositi

1 reference

12 December 2020

Numerical chromosome abnormalities in the spermatozoa of the fathers of children with trisomy 21 of paternal origin: generalised tendency to meiotic non-disjunction

1 reference

12 December 2020

The distal triradius t on the hands of parents and sibs of mongol imbeciles

1 reference

12 December 2020

Paternal gonadal mosaicism detected in a couple with recurrent abortions undergoing PGD: FISH analysis of sperm nuclei proves valuable

1 reference

12 December 2020

Investigation of factors associated with paternal nondisjunction of chromosome 21

1 reference

12 December 2020

The somatic chromosomes in mongolism

1 reference

12 December 2020

Paternal nondisjunction in trisomy 21: excess of male patients

1 reference

12 December 2020

Intra-individual and inter-individual variations in sperm aneuploidy frequencies in normal men

1 reference

12 December 2020

Paternal normal-trisomy 21 mosaicism as an indication for amniocentesis

1 reference

12 December 2020

Dermatoglyphic and cytogenetic studies in parents of children with trisomy 21

1 reference

12 December 2020

Somatic pairing of chromosome 1 centromeres in interphase nuclei of human cerebellum

1 reference

12 December 2020

Trisomy 21 Down syndrome. Parental mosaicism

1 reference

12 December 2020

Role of mitotic control in spermatogenesis

1 reference

12 December 2020

Reproduction in Down syndrome

1 reference

12 December 2020

Lack of aneuploidy for chromosomes 15, 16, and 18 in placentas from small-for-gestational-age liveborn infants

1 reference

12 December 2020

Investigation of 142 mosaic mongols and mosaic parents of mongols; cytogenetic analysis and maternal age at birth

1 reference

12 December 2020

Space-time analysis of Down syndrome: results consistent with transient pre-disposing contagious agent

1 reference

12 December 2020

Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring

1 reference

12 December 2020

Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases

1 reference

12 December 2020

Maternal smoking as a cause of mosaic aneuploidy in spontaneous abortions

1 reference

12 December 2020

Identifiers

DOI

10.1186/1755-8166-3-4

1 reference

29 July 2017

1 reference

29 July 2017

1 reference