Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature (Q38098725)

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scientific article published on June 1990

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Language	Label	Description	Also known as
English	Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature	scientific article published on June 1990

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

title

Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature (English)

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stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

main subject

heterozygosity

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inferred from title

author name string

F Pellestor

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

publication date

1 June 1990

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stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

published in

Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

volume

85

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

page(s)

49-54

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stated in

Europe PubMed Central

PubMed publication ID

2358303

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28 August 2017

cites work

Segregation of chromosomes into the spermatozoa of a man heterozygous for a 14;21 Robertsonian translocation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic and synaptonemal complex studies in a 14/21 translocation carrier

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

Trisomy 13 in the child of two carriers of a 13/15 translocation

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterility

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

[Demonstration of human spermatozoa chromosomes in a heterospecific system: technical difficulties]

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

Pachytene analysis of a man with a 13q;14q translocation and infertility. Behavior of the trivalent and nonrandom association with the sex vesicle

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

Breeding studies reveal segregation of a canine Robertsonian translocation along Mendelian proportions

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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Structural rearrangements in the parents of children with primary trisomy 21.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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Direct segregation analysis of reciprocal translocations: a study of 283 sperm karyotypes from four carriers

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

Analysis of meiotic segregation in a man heterozygous for two reciprocal translocations using the hamster in vitro penetration system.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

Structural basis for Robertsonian translocations in man: association of ribosomal genes in the nucleolar fibrillar center in meiotic spermatocytes and oocytes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

A cytogenetic survey of 14,069 newborn infants. III. an analysis of the significance and cytologic behavior of the Robertsonian and reciprocal translocations

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prevalence of translocations in parents of children with regular trisomy 21: a possible interchromosomal effect?

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three generations and six family members with a t(13q15q) chromosome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

The meiotic consequences of chromosome modifications

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary hypogonadism and 13/15 chromosome translocation in Prader-Labhart-Willi syndrome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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inferred from PubMed ID database lookup

The nonrandom participation of human acrocentric chromosomes in Robertsonian translocations

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Down's syndrome. Current stage of cytogenetic research

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiosis and spermatogenesis in bulls heterozygous for a presumptive 1/29 Robertsonian translocation

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic analysis of sperm from a male heterozygous for a 13;14 Robertsonian translocation

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Random acrocentric bivalent associations in human pachytene spermatocytes. Molecular implications in the occurrence of Robertsonian translocations

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aneuploid spermatocyte frequency in domestic sheep heterozygous for three Robertsonian translocations

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

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The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reproductive risk of t(13q14q) carriers: Case report and review

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

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Study of progeny of individuals bearing a t(DqDq) translocation

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

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Mutation rates of structural chromosome rearrangements in man.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

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Analysis of translocations observed in three different populations. II. Robertsonian translocations

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

retrieved

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic 14 trisomy in a female child with multiple abnormalities

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/2358303

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A collaborative study of the segregation of inherited chromosome structural rearrangements in 1356 prenatal diagnoses

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2358303

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00276325

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

Dimensions Publication ID

1031327488

0 references

PubMed publication ID

2358303

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2358303

retrieved

28 August 2017

 

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