(Q40342284)

19 September 2017

title

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

1 reference

19 September 2017

Kelley RI

1

1 reference

19 September 2017

Zackai EH

2

1 reference

19 September 2017

Emanuel BS

3

1 reference

19 September 2017

Kistenmacher M

4

1 reference

19 September 2017

Greenberg F

5

1 reference

19 September 2017

Punnett HH

6

1 reference

19 September 2017

language of work or name

English

0 references

publication date

1 August 1982

1 reference

The Journal of Pediatrics

19 September 2017

published in

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19 September 2017

volume

101

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19 September 2017

issue

2

1 reference

19 September 2017

page(s)

197-200

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Familial thymic aplasia. Attempted reconstitution with fetal thymus in a Millipore diffusion chamber

19 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

A deletion in chromosome 22 can cause DiGeorge syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

The spectrum of the DiGeorge syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

Monosomy of chromosome No. 22. A case report.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

Translocation 4p-- syndrome: a general review

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

Structural aberrations of the long arm of chromosome no. 22. Report fo a family with translocation t(11;22) (q25;q11).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

inferred from DOI database lookup

7 January 2021

based on heuristic

Three translocations involving C- or G-group chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2882%2980116-9

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-3476(82)80116-9

1 reference

19 September 2017

1 reference