(Q67435376)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1248832%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

title

A boy with 47,X,del(X)(p11leads to q13:q21leads to q24),del(Y)(q11):reexamination of a case previously described as 47,XX,?Yq- (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1248832%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

main subject

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1248832

chromosomal deletion syndrome

5 September 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1248832

5 September 2022

J. Nielsen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1248832

5 September 2022

K. Rasmussen

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1248832

5 September 2022

I. Sillesen

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1248832

5 September 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=1248832

5 September 2022

publication date

1 February 1976

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1248832%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

29 February 1976

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1248832

5 September 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1248832%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

volume

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1248832%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1248832%20AND%20SRC:MED&resulttype=core&format=json

13 September 2019

page(s)

227-230

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1248832%20AND%20SRC:MED&resulttype=core&format=json

Klinefelter's syndrome with a presumptive deleted X chromosome.

13 September 2019

cites work

1 reference

12 December 2020

1 reference

12 December 2020

A 47,XXq-Y Klinefelter male

1 reference

12 December 2020

Center for Barr body condensation on the proximal part of the human Xq: a hypothesis

1 reference

12 December 2020

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

1 reference

12 December 2020

[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020