(Q69832588)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

title

Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

main subject

Prader–Willi syndrome

1 reference

1 reference

N Niikawa

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

S Ishikiriyama

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

publication date

1 January 1985

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

volume

69

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

page(s)

22-27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3855404%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00295524

6 October 2019

exact match

0 references

cites work

Unmasking of heterozygosity by inherited balanced translocations. Implications for prenatal diagnosis and gene mapping

1 reference

12 December 2020

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

1 reference

12 December 2020

Cytogenetic studies of familial Prader-Willi syndrome

1 reference

12 December 2020

The cytogenetic controversy in the Prader-Labhart-Willi syndrome

1 reference

12 December 2020

Parental origin of de novo chromosome rearrangements

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

Prader-Willi syndrome associated with inversion of chromosome 15

1 reference

12 December 2020

The Prader-Willi syndrome and interstitial deletion of chromosome 15: high-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants

1 reference

12 December 2020

Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases

1 reference

12 December 2020

Site-specific X-chromosome rearrangements from hybrid dysgenesis in Drosophila melanogaster

1 reference

12 December 2020

Translocations in Prader-Willi syndrome.

1 reference

12 December 2020

Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

1 reference

12 December 2020

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

1 reference

12 December 2020