(Q71259725)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

title

Familial DiGeorge syndrome and associated partial monosomy of chromosome 22 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

1 reference

F Greenberg

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

W E Crowder

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

V Paschall

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

J Colon-Linares

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

B Lubianski

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

D H Ledbetter

6

1 reference

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17 October 2019

publication date

1 January 1984

1 reference

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17 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

volume

65

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

page(s)

317-319

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00291554

17 October 2019

exact match

0 references

cites work

A deletion in chromosome 22 can cause DiGeorge syndrome

1 reference

12 December 2020

Radioimmunoassay for the middle region of human parathyroid hormone using an homologous antiserum with a carboxy-terminal fragment of bovine parathyroid hormone as radioligand

1 reference

12 December 2020

Partial monosomy 22 as the result of an unbalanced translocation 5:22 in a patient with cri-du-chat syndrome

1 reference

12 December 2020

The spectrum of the DiGeorge syndrome

1 reference

12 December 2020

Translocation 4p-- syndrome: a general review

1 reference

12 December 2020

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

1 reference

12 December 2020

The association of the DiGeorge anomalad with partial monosomy of chromosome 22.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00291554

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6693120%20AND%20SRC:MED&resulttype=core&format=json

17 October 2019

1 reference