(Q35245848)

7 August 2017

On the origin of chromosome anomaly (English)

1 reference

7 August 2017

Magenis RE

1

1 reference

PubMed ID

2964777

7 August 2017

language of work or name

English

0 references

publication date

1 April 1988

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

42

1 reference

7 August 2017

4

1 reference

7 August 2017

529-533

1 reference

The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Parental alpha 1-antitrypsin (PI) types and meiotic nondisjunction in the aetiology of Down syndrome.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Maternal age and origin of non-disjunction in trisomy 21.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Trisomy 21: origin of non-disjunction.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

21 p-maternal in duplicate in a case of trisomy 21

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Paternal trisomy 21 mosaicism and Down's syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Familial predisposition to thyroid disease in Down's syndrome: controlled immunoclinical studies.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Mongolism, delayed fertilization and human sexual behaviour

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Virus aetiology for Down's syndrome (mongolism).

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Maternal radiation and chromosomal aberrations

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Accelerated ageing in young mothers of children with Down's syndrome.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Parental origin of the extra chromosome in the cat eye syndrome: evidence from heteromorphism and in situ hybridization analysis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Cytogenetic and molecular analysis of sex-chromosome monosomy

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Cytogenetic and molecular studies of trisomy 13.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Hydatidiform mole: two entities. A morphologic and cytogenetic study with some clinical consideration

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Parthenogenic Origin of Benign Ovarian Teratomas

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Origin of the extra chromosome in trisomy 21

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Preferential maternal derivation in inv dup(15): analysis of eight new cases.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715222

Dermatoglyphic and cytogenetic studies in parents of children with trisomy 21

15 November 2018

1 reference

12 December 2020

Non-disjunction in trisomy 21: study of chromosomal heteromorphisms in 110 families

1 reference

12 December 2020

Parental origin of chromosomes in Down's syndrome

1 reference

12 December 2020

The origin of human trisomy: a study of heteromorphisms and satellite associations

1 reference

12 December 2020

Seasonality of pre-ovulatory non-disjunction and the aetiology of Down syndrome. A European collaborative study

1 reference

12 December 2020

Source of single X in XO Turner syndrome: a comment

1 reference

12 December 2020

A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes

1 reference

12 December 2020

Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe

1 reference

12 December 2020

The Christchurch chromosome (Gp-). Mongolism, erythroleukemia and an inherited Gp- chromosome (Christchurch)

1 reference

12 December 2020

Analysis of human metaphase chromosome set by aid of DNA-binding fluorescent agents

1 reference

12 December 2020

Distinction between extra G-like chromosomes by quinacrine mustard fluorescence analysis

1 reference

12 December 2020

Month of birth and gametopathy. An investigation into patients with Down's, Klinefelter's and Turner's syndrome

1 reference

12 December 2020

Induction of chromosomal errors

1 reference

12 December 2020

Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+

1 reference

12 December 2020

Trisomy 21 in man due to maternal non-disjunction during the first meiotic division

1 reference

12 December 2020

Origin of triploidy and tetraploidy in man: 11 cases with chromosome markers

1 reference

12 December 2020

Identifiers

PMCID

1715222

1 reference

7 August 2017

1 reference

PubMed ID

2964777