Partial deletion of the X chromosome in gonadal dysgenesis 46,X,del(X)(p22) identified by BudR treatment (Q67436928)

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scientific article published on December 29, 1978

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Language	Label	Description	Also known as
English	Partial deletion of the X chromosome in gonadal dysgenesis 46,X,del(X)(p22) identified by BudR treatment	scientific article published on December 29, 1978

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

title

Partial deletion of the X chromosome in gonadal dysgenesis 46,X,del(X)(p22) identified by BudR treatment (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

main subject

gonadal dysgenesis

1 reference

based on heuristic

inferred from title

chromosomal deletion syndrome

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738735

retrieved

24 July 2022

author name string

P. Petrinelli

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738735

retrieved

24 July 2022

A. Antonelli

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738735

retrieved

24 July 2022

P. Gabellini

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738735

retrieved

24 July 2022

F. Gigliani

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738735

retrieved

24 July 2022

L. Marcucci

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738735

retrieved

24 July 2022

B. Nicoletti

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A738735

retrieved

24 July 2022

language of work or name

English

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

738735

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=738735

retrieved

24 July 2022

publication date

1 December 1978

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

29 December 1978

1 reference

stated in

National Center for Biotechnology Information

PubMed publication ID

738735

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=738735

retrieved

24 July 2022

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

volume

45

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

page(s)

351-354

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

cites work

New technique for distinguishing between human chromosomes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/738735

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal X chromosomes in man: Origin, behavior and effects

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/738735

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Karyotype-phenotype correlation in a 46,Xdel(X) (p22) diagnosis (author's transl)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/738735

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Partial deletion of the short arm of an X chromosome]

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/738735

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Short arm deletion of an X chromosome, 46,XXp-

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/738735

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Letter: Cytogenetic evidence for evolution of X-chromosome inactivation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/738735

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Women heterozygous for deficiency of the (p21 ? pter) region of the X chromosome are fertile

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/738735

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/738735

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00278734

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

Dimensions Publication ID

1020081100

0 references

PubMed publication ID

738735

1 reference

stated in

Europe PubMed Central

PubMed publication ID

738735

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:738735%20AND%20SRC:MED&resulttype=core&format=json

retrieved

13 September 2019

 

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