(Q56383962)

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A paternal wash in Apert syndrome

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scholarly article

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A paternal wash in Apert syndrome (English)

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C Sapienza

1

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publication date

May 1996

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Nature Genetics

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13

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1

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9-10

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https://scigraph.springernature.com/pub.10.1038/ng0596-9

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Exclusive paternal origin of new mutations in Apert syndrome

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

7 January 2021

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

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

7 January 2021

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

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

7 January 2021

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

1 reference

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

7 January 2021

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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

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

7 January 2021

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Imprinting: a gamete's point of view

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

7 January 2021

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Focus on genome imprinting

1 reference

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

7 January 2021

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

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

7 January 2021

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

1 reference

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

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

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

7 January 2021

based on heuristic

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Identifiers

10.1038/NG0596-9

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