(Q35197568)

7 August 2017

Parental origin of the extra chromosome in trisomy 18. (English)

1 reference

7 August 2017

K G Kupke

1

1 reference

PubMed ID

2577470

7 August 2017

U Müller

series ordinal

2

1 reference

PubMed ID

2577470

7 August 2017

language of work or name

English

0 references

publication date

1 October 1989

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

45

1 reference

7 August 2017

599-605

1 reference

7 August 2017

4

1 reference

Rates of chromosome abnormalities at different maternal ages.

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

A strategy to reveal high-frequency RFLPs along the human X chromosome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Survival in trisomy 18. Life tables for use in genetic counselling and clinical paediatrics.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Moderately repeated DNA sequences specific for the short arm of the human Y chromosome are present in XX males and reduced in copy number in an XY female

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Trisomy 18 in a 13 year old girl

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Variable number of tandem repeat (VNTR) markers for human gene mapping

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

The heteromorphic marker on chromosome 18 using restriction endonuclease AluI.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Cytogenetic and molecular studies of trisomy 13.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

The probability of detecting the origin of nondisjunction of autosomal trisomies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Incidence of chromosome aberrations among 11 148 newborn children

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Clinical experience with trisomies 18 and 13

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

A prospective psychological and cytogenetic study of three girls with mosaic mongolism

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Parental origin of the extra chromosome in Down's syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683505

Twelve loci form a continuous linkage map for human chromosome 18

28 July 2018

1 reference

12 December 2020

Decreasing mosaicism in Down's syndrome

1 reference

12 December 2020

Origin of extra chromosome in Patau syndrome

1 reference

12 December 2020

Reduced recombination rate on chromosomes 21 that have undergone nondisjunction

1 reference

12 December 2020

Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18

1 reference

12 December 2020

Origin of the extra chromosome in trisomy 18. A study on five patients using a restriction fragment length polymorphism

1 reference

12 December 2020

Identifiers

PMCID

1683505

1 reference

7 August 2017

1 reference

PubMed ID

2577470