(Q33596715)

28 July 2017

1 reference

title

On the parental origin of de novo mutation in man. (English)

1 reference

28 July 2017

Chandley AC

1

1 reference

PubMed ID

1677423

28 July 2017

language of work or name

English

0 references

publication date

1 April 1991

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

28

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28 July 2017

4

1 reference

28 July 2017

217-223

1 reference

Radiosensitivity at Specific Autosomal Loci in Mature Sperm and Spermatogonial Cells of Drosophila Melanogaster

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Modification of X-Ray Mutagenesis in Drosophila. I. Reunion of Chromosomes Irradiated during Spermiogenesis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Parental age and mutation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Effect of maternal age on autosomal trisomies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Cytogenetic effects of X-rays and fission neutrons in female mice.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Klinefelter's syndrome: an analysis of the origin of the additional sex chromosome using molecular probes.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Cytogenetic and molecular analysis of sex-chromosome monosomy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Cytogenetic and molecular studies of trisomy 13.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Chlorambucil effectively induces deletion mutations in mouse germ cells

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Parental origin of the extra chromosome in trisomy 18.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

The parental origin of the extra X chromosome in 47,XXX females.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Genetic and molecular analysis of chlorambucil-induced germ-line mutations in the mouse

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Parental age and seasonal variation in the births of children with sporadic retinoblastoma: a mutation-epidemiologic study.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Genomic imprinting: review and relevance to human diseases.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Parental origin of de novo constitutional deletions of chromosomal band 11p13

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Classification and relationships of induced chromosomal structual changes

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Xg groups and sex chromosome abnormalities in people of northern European ancestry: an addendum

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Mutation frequencies in female mice and the estimation of genetic hazards of radiation in women

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Spermatogenesis in man: an estimate of its duration.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Preferential germline mutation of the paternal allele in retinoblastoma

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016821

Parental origin of chromosome 5 deletions in the cri-du-chat syndrome

30 October 2018

1 reference

12 December 2020

Reduced recombination rate on chromosomes 21 that have undergone nondisjunction

1 reference

12 December 2020

Gamma-ray-induced numerical and structural chromosome anomalies in mouse immature oocytes

1 reference

12 December 2020

Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome

1 reference

12 December 2020

The volumes and morphology of human chromosomes in mitotic reconstructions

1 reference

12 December 2020

Parental origin of mutations of the retinoblastoma gene

1 reference

12 December 2020

Consistent involvement of only 71 of the 329 chromosomal bands of the human genome in primary neoplasia-associated rearrangements

1 reference

12 December 2020

Sister chromatid exchange analysis in lung and peripheral blood lymphocytes of mice exposed to methyl isocyanate by inhalation

1 reference

12 December 2020

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability

1 reference

12 December 2020

Definition of functional units in a small chromosomal segment of the mouse and its use in interpreting the nature of radiation-induced mutations

1 reference

12 December 2020

Xg and sex-chromosome abnormalities

1 reference

12 December 2020

Autosomal Translocations Causing Male Sterility and Viable Aneuploidy in the Mouse

1 reference

12 December 2020

Genetic analysis of induced deletions and of spontaneous nondisjunction involving chromosome 2 of the mouse

1 reference

12 December 2020

Colour-blindness in Klinefelter's Syndrome

1 reference

12 December 2020

Parental origin of autosomal trisomies

1 reference

12 December 2020

Parental origin of de novo chromosome rearrangements

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.28.4.217

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

PubMed ID

1677423