(Q40854163)

24 September 2017

1 reference

title

Wilms tumor in a patient with Prader-Willi syndrome (English)

1 reference

24 September 2017

Coppes MJ

1

1 reference

24 September 2017

Sohl H

2

1 reference

24 September 2017

Teshima IE

3

1 reference

24 September 2017

Mutirangura A

4

1 reference

24 September 2017

Ledbetter DH

5

1 reference

24 September 2017

Weksberg R

6

1 reference

24 September 2017

language of work or name

English

0 references

publication date

1 May 1993

1 reference

The Journal of Pediatrics

24 September 2017

1 reference

24 September 2017

122

1 reference

24 September 2017

730-733

1 reference

24 September 2017

5 Pt 1

1 reference

Second Annual Prader-Willi Syndrome Scientific Conference. Houston, June 17, 1987. Proceedings and abstracts

24 September 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

Genomic imprinting and carcinogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

7 January 2021

Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

Leukaemia and the Prader-Willi syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

Prader Willi syndrome and testicular tumour

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

Genomic imprinting and genetic disorders in man.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

Parental origin of chromosomes involved in the translocation t(9;22).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2806%2980015-6

10.1016/S0022-3476(06)80015-6

7 January 2021

Identifiers

DOI

1 reference

24 September 2017

1 reference