(Q36291111)

13 August 2017

1 reference

title

Differentiated recurrence risk estimations in the Prader-Willi syndrome (English)

1 reference

13 August 2017

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

16 October 2022

author name string

I. Kennerknecht

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1623627

16 October 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1623627

16 October 2022

publication date

1 June 1992

1 reference

full work available at URL

13 August 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.1992.tb03403.x

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1992.tb03403.x/fullpdf

16 October 2022

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

16 October 2022

1 reference

13 August 2017

41

1 reference

13 August 2017

303-308

1 reference

13 August 2017

6

1 reference

Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences

13 August 2017

3

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prevalence study of Prader-Willi syndrome in North Dakota

16 October 2022

4

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Familial Prader-Willi syndrome

16 October 2022

5

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

16 October 2022

6

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

16 October 2022

7

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prader-Willi syndrome: current understanding of cause and diagnosis

16 October 2022

8

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Recurrence risk in Prader-Willi syndrome

16 October 2022

9

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Differential activity of maternally and paternally derived chromosome regions in mice

16 October 2022

11

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Translocations in Prader-Willi syndrome.

16 October 2022

12

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prader-Willi syndrome. Variable severity and recurrence risk

16 October 2022

13

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry

16 October 2022

14

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Familial Prader-Willi syndrome

16 October 2022

15

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome

16 October 2022

16

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

16 October 2022

17

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prader-Willi syndrome and prenatal diagnosis

16 October 2022

18

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prader-Willi syndrome in siblings, due to unbalanced translocation between chromosomes 15 and 22.

16 October 2022

19

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

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.

16 October 2022

20

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

The Prader-Willi syndrome and the Sotos syndrome: syndromes or sequences?

16 October 2022

21

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Risk of recurrence in usually nongenetic malformation syndromes

16 October 2022

23

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Deletions of proximal 15q without Prader-Willi syndrome.

16 October 2022

24

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Adults with Prader-Willi syndrome: a survey of 232 cases

16 October 2022

26

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR

16 October 2022

27

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Cytogenetic studies of familial Prader-Willi syndrome

16 October 2022

29

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Cytogenetic and molecular study of Angelman syndrome

16 October 2022

32

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.

16 October 2022

34

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prader-Willi syndrome and Sotos syndrome

16 October 2022

35

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR)

16 October 2022

36

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Molecular and clinical overlap of Angelman and Prader-Willi syndrome phenotypes

16 October 2022

37

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

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

16 October 2022

39

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

On the parental origin of the deletion in Angelman syndrome

16 October 2022

40

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prenatal diagnosis of del(15)(q11q13)

16 October 2022

43

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

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

16 October 2022

44

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

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

16 October 2022

45

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Familial Prader-Willi syndrome with apparently normal chromosomes

16 October 2022

46

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Is Angelman syndrome an alternate result of del(15)(q11q13)?

16 October 2022

47

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

16 October 2022

48

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis

16 October 2022

49

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome

16 October 2022

52

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

16 October 2022

53

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

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

16 October 2022

54

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

The association of Angelman's syndrome with deletions within 15q11-13

16 October 2022

56

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Genomic imprinting determines methylation of parental alleles in transgenic mice

16 October 2022

58

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes

16 October 2022

61

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prenatal diagnosis and the Prader-Willi syndrome

16 October 2022

62

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

16 October 2022

63

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

The Prader-Willi syndrome: neuroendocrine study of identical twins

16 October 2022

65

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion

16 October 2022

66

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons

16 October 2022

67

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

16 October 2022

69

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

Prader-Willi syndrome associated with inversion of chromosome 15

16 October 2022

70

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.1992.TB03403.X

16 October 2022

Identifiers

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1623627

16 October 2022

1 reference