(Q35196939)

7 August 2017

1 reference

title

Twinning and mitotic crossing-over: some possibilities and their implications (English)

1 reference

7 August 2017

Côté GB

1

1 reference

7 August 2017

Gyftodimou J

series ordinal

2

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 July 1991

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

49

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7 August 2017

issue

1

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7 August 2017

page(s)

120-130

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Somatic Crossing over and Segregation in Drosophila Melanogaster

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Malformations unique to the twinning process.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Twinning rate in spontaneous abortions

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Monozygotic twins of different sex

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

A study of monozygous quadruplet armadillos in relation to mammalian inheritance

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Colour vision deficiency in one of two presumably monozy?otic twins with secondary amenorrhoea

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Origin and Clinical Significance of Twinning

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligence

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Differential activity of maternally and paternally derived chromosome regions in mice

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

IVF and Goldenhar 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=1683204

The "vanishing twin": ultrasonographic assessment of fetal disappearance in the first trimester

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Homologous chromosome recombination generating immunoglobulin allotype and isotype switch variants

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Discordance in a pair of identical twin carriers of factor IX deficiency

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Hypothyroidism and sex chromosomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Goldenhar complex in discordant monozygotic twins: a case report and review of the literature

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Contiguous gene syndromes: a component of recognizable syndromes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Zygosity determination in newborn twins using DNA variants

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/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=1683204

Genetic aspects of tuberous sclerosis in the west of Scotland

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Uniparental disomy as a mechanism for human genetic disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Duchenne muscular dystrophy in one of monozygotic twin girls

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi 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=1683204

Chromosome maps of man and mouse. IV.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Asymmetry in chromosome pairing: a major factor in de novo mutation and the production of genetic disease in man

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Isodisomy of chromosome 7 in a patient with cystic fibrosis: could uniparental disomy be common in humans?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Monozygotic twins discordant for the Russell-Silver 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=1683204

Detrimental effects of two active X chromosomes on early mouse development.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Thyroid function in patients with Down syndrome: preliminary results from non-institutionalized patients in the Veneto region

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

28 July 2018

Sex ratio in twin births

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Somatic recombination as possible prelude to malignant transformation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Monozygotic twinning and structural defects

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Satellite DNA and heterochromatin variants: The case for unequal mitotic crossing over

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Chromosome polymorphism and twin zygosity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Epiloia in twins: a problem in diagnosis and counselling

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Polymporphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing over

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Overripeness of the egg as a cause of twinning and teratogenesis: a review

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Asymmetry and discordance for congenital anomalies in conjoined twins: a report of six cases.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Genomic imprinting determines methylation of parental alleles in transgenic mice

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Part II. Amyoplasia: Twinning in amyoplasia—a specific type of arthrogryposis with an apparent excess of discordantly affected identical twins

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Association of amyoplasia with gastroschisis, bowel atresia, and defects of the muscular layer of the trunk

15 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683204

Paternal preponderance in familial Parkinson's disease

15 November 2018

1 reference

12 December 2020

Monochorionic diamniotic minimally conjoined twins: a case report

1 reference

12 December 2020

The zygosity determination of Japanese twins using a minisatellite core probe

1 reference

12 December 2020

A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13

1 reference

12 December 2020

Cytological demonstration of mitotic crossing-over in man

1 reference

12 December 2020

Influence of parental chromosomes on spatial specificity in androgenetic ↔ parthenogenetic chimaeras in the mouse

1 reference

12 December 2020

On the timing of monozygotic twinning events

1 reference

12 December 2020

Monozygotic female twin carriers discordant for the clinical manifestations of Duchenne muscular dystrophy

1 reference

12 December 2020

Fetal abnormality (Goldenhar syndrome) occurring in one of triplet infants derived from in vitro fertilization with possible monozygotic twinning

1 reference

12 December 2020

Molecular nature of in vivo mutations in human cells at the autosomal HLA-A locus

1 reference

12 December 2020

The cis-trans effects of crossing-over on the penetrance and expressivity of dominantly inherited disorders

1 reference

12 December 2020

Genetic aspects of hemifacial microsomia

1 reference

12 December 2020

Congenital malformations in twins: a population study

1 reference

12 December 2020

Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins

1 reference

12 December 2020

Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours

1 reference

12 December 2020

Genetic aspects of hemifacial microsomia

1 reference

12 December 2020

Chromosomal aberrations in embryos from overripe eggs

1 reference

12 December 2020

Genetic analysis based on mitotic recombination

1 reference

12 December 2020

Use of minisatellite DNA probes for determination of twin zygosity at birth

1 reference

12 December 2020

Discordance of signs in monozygotic twins concordant for the goldenhar anomaly

1 reference

12 December 2020

Segregation after mitotic crossing-over in isodicentric X chromosomes

1 reference

12 December 2020

Identifiers

PMC publication ID

1683204

1 reference

7 August 2017

1 reference