(Q40323919)

English

Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature

scientific article published on January 1981

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

1 reference

Europe PubMed Central

Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

author name string

D P Duckett

1

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

S H Roberts

2

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

publication date

1 January 1981

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

58

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

377-386

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Systematic analysis of 95 reciprocal translocations of autosomes

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Structural differences in reciprocal translocations. Potential for a model of risk in Rcp

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Localisation of the human ABO: Np-1: AK-1 linkage group by regional assignment of AK-1 to 9q34.

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Ring chromosome 15 syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Chiasma distribution at diakinesis in the normal human male

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Ring chromosome 15: phenotype, Ag-NOR analysis, secondary aneuploidy, and associated chromosome instability

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Genetics of the +p9 syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Glossary of Genetics and Cytogenetics – Classical and Molecular

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Analysis of banding patterns and mosaic configurations in a case of ring chromosome 15.

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

A (1;15) translocation, balanced, 46 chromosomes. Repository identification No. GM-126

1 reference

https://api.crossref.org/works/10.1007%2FBF00282819

21 January 2018

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PARTIAL TRISOMY-DEFICIENCY SYNDROME RESULTING FROM A RECIPROCAL TRANSLOCATION IN A LARGE KINDRED

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trial classification of D group chromosome long arm deletions. Apropos of a 15q- case

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of deletion of short arm satellites in acrocentric chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

T (14q-; 21q + ) translocation in the father. Partial trisomy 14 and monosomy 21 in the daughter

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

15/15 translocation in Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Partial trisomy (10pter leads to 10q21) and partial monosomy (21pter leads to 21q21) due to a reciprocal balanced familial translocation (10;21)(q21;q21) (author's transl)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tertiary trisomy 14: is there a syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 9p resulting from maternal 9/21 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial translocation t(10;21)(q22;q22)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reciprocal translocations in man. 3:1 Meiotic disjunction resulting in 47- or 45-chromosome offspring

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 6/15 translocation with multiple congenital anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a D/E(15/18) translocation chromosome by quinacrine fluorescence and Urea banding techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome segregation in translocations involving chromosome 6 in maize

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new case of rearrangement of chromosome 15 associated with Prader Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new translocation between chromosomes in the 6-12 and 21-22 groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reciprocal translocations

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two reciprocal translocations t(9p+;13q-) and t(13q-;21q+): a study of the families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further Identification of a D/E Translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proximal 14 trisomy 46,XX, -22 +der(14)t(14;22) (q21;q11)mat

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of genetic disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tandem translocation 15-13

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal karyotype analysis in high risk families

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A ring 15 chromosome in a girl with minor abnormalities.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autoradiographic studies on X-autosomal translocation in man: 45,X.15-,tan(15qZq+)+

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Prader-Willi syndrome with a 15/3 translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translocation of 9q/13q resulting in duplication (trisomy 9pter leads to 9q22) and deficiency (monosomy 13pter leads to 13q12)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Translocation 46,XX, t(15; 21) (q13; q22,1) in the mother of 2 children with partial trisomy 15 and monosomy 21]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A rapid banding technique for human chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

(6;15) Translocation with loss of chromosome material in the patient and various chromosome aberrations in family members

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four cases of 9p trisomy resulting from a balanced familial translocation (9:15) (q13;q11). Clinical picture and cytogenetic findings.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring chromosome 15 in a male adult with radial defects. Evaluation of the phenotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trisomy 4p. Three new observations (author's transl)

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital heart disease with del(15q) mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ring chromosome 15 and failure to thrive

1 reference

https://pubmed.ncbi.nlm.nih.gov/7035334

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00282819

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q40323919&oldid=2203602807"