A paternal wash in Apert syndrome (Q56383962)

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Language	Label	Description	Also known as
English	A paternal wash in Apert syndrome	No description defined

Statements

instance of

scholarly article

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title

A paternal wash in Apert syndrome (English)

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main subject

Apert syndrome

1 reference

based on heuristic

inferred from title

author name string

C Sapienza

series ordinal

1

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language of work or name

English

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publication date

May 1996

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published in

Nature Genetics

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volume

13

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issue

1

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page(s)

9-10

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cites work

Exclusive paternal origin of new mutations in Apert syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A study of parental age effects on the occurrence of fresh mutations for the Apert syndrome.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Sex difference in methylation of single-copy genes in human meiotic germ cells: Implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Imprinting: a gamete's point of view

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Focus on genome imprinting

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Further evidence of no linkage between schizophrenia and the dopamine D3 receptor gene locus

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

GENETIC TESTS WITH A SEX-LINKED MARKER: GLUCOSE-6-PHOSPHATE DEHYDROGENASE

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNG0596-9

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG0596-9

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PubMed publication ID

8673111

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