(Q35202668)

English

The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

Van Dyke DL

1

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Weiss L

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Roberson JR

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Babu VR

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

language of work or name

0 references

publication date

1 March 1983

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

35

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

301-308

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Mutation rates of structural chromosome rearrangements in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Acceptance of amniocentesis by low-income patients in an urban hospital.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Utilization of prenatal genetic diagnosis in women 35 years of age and older in the United States, 1977 to 1978.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Prenatal chromosomal diagnosis. Racial and geographic variation for older women in Georgia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

A cytogenetic survey of 11,680 newborn infants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Incidence and mutation rates of structural rearrangements of the autosomes in man.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Translocations of D chromosomes in two families: t(13q14q) and t(13q14q)+(13p14p)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Incidence of chromosome aberrations among 11 148 newborn children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

The chromosomal basis of human infertility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Prenatal Genetic Diagnosis in 3000 Amniocenteses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Chromosome analysis on 930 consecutive newborn children using quinacrine fluorescent banding technique

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685549

13 July 2018

Chromosome aberrations in 2159 consecutive newborn babies

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome abnormalities in newborn children. Aetiological aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal Abnormalities in the Human Population: Estimation of Rates Based on New Haven Newborn Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Male infertility and 13-14 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome studies in 5,049 consecutive newborn children

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A G-band study of chromosomes in liveborn infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome findings in 2,500 second trimester amniocenteses

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

All patients with acute nonlymphocytic leukemia may have a chromosomal defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Massachusetts Department of Public Health. Use of prenatal cytogenetic diagnosis in New York State

1 reference

https://pubmed.ncbi.nlm.nih.gov/6837576

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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