(Q38551301)

4 September 2017

A new case of trisomy for the distal part of 13q due to maternal translocation, t(9;13)(p21;q21) (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964983

human chromosomes 6-12 and X

10 August 2022

main subject

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964983

10 August 2022

human chromosomes 13-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964983

10 August 2022

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964983

10 August 2022

trisomy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964983

chromosomal translocation

10 August 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964983

10 August 2022

author name string

M. Jotterand

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964983

10 August 2022

E. Juillard

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A964983

10 August 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=964983

10 August 2022

publication date

1 August 1976

1 reference

4 September 2017

30 August 1976

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=964983

10 August 2022

1 reference

4 September 2017

33

1 reference

4 September 2017

213-222

1 reference

4 September 2017

3

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00286845

4 September 2017

0 references

cites work

NUCLEAR ABNORMALITIES OF THE NEUTROPHILS IN D1 (13-15)-TRISOMY SYNDROME

1 reference

12 December 2020

DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY SYNDROME

1 reference

12 December 2020

Chromosome preparations of leukocytes cultured from human peripheral blood

1 reference

12 December 2020

[Partial 13 trisomy by maternal 46, XX, t (3; 13) (p 26; q 21) translocation]

1 reference

12 December 2020

A family with balanced D1?Cs-translocation carriers and unbalanced offspring

1 reference

12 December 2020

Different forms of incomplete trisomy 13. Mosaicism and partial trisomy for the proxim

1 reference

12 December 2020

Inherited translocations in two families (t(14q+;10q-) and t(13q-;21q+)).

1 reference

12 December 2020

Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome

1 reference

12 December 2020

An inherited chromosome aberration in a girl with signs of de Lange syndrome

1 reference

12 December 2020

Localization of genes on chromosome 13: analysis of two kindreds

1 reference

12 December 2020

Trisomy for the distal segment of chromosome 13: a new syndrome

1 reference

12 December 2020

Inherited pericentric inversion of a group D (13-15) chromosome

1 reference

12 December 2020

Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

Duplication/deficiency product of a pericentric inversion in man: A cause of D1 trisomy syndrome

1 reference

12 December 2020

Deoxyribonucleic acid replication and mapping of the D-1 chromosome. A study of two patients with partial trisomy D-1

1 reference

12 December 2020

An unusual partial trisomy 13

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00286845

1 reference

Dimensions Publication ID

4 September 2017

0 references

1 reference