(Q21090070)

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The role of inbreeding in the extinction of a European royal dynasty

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The Role of Inbreeding in the Extinction of a European Royal Dynasty

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The role of inbreeding in the extinction of a European royal dynasty (English)

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Francisco C Ceballos

2

Francisco C

Ceballos

1 reference

11 July 2022

Gonzalo Alvarez

1

Gonzalo

Alvarez

1 reference

11 July 2022

Celsa Quinteiro

series ordinal

3

author given names

Celsa

author last names

Quinteiro

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11 July 2022

language of work or name

English

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publication date

2009

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published in

PLOS One

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volume

4

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issue

4

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page(s)

e5174

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copyright license

Creative Commons Attribution 4.0 International

start time

15 April 2009

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

1 reference

stated in

PubMed Central

reference URL

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19 March 2017

Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion

1 reference

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PubMed Central

reference URL

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19 March 2017

The costs of human inbreeding and their implications for variations at the DNA level

1 reference

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PubMed Central

reference URL

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retrieved

19 March 2017

Reproductive behavior and health in consanguineous marriages

1 reference

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PubMed Central

reference URL

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retrieved

19 March 2017

Hypothalamic and pituitary development: novel insights into the aetiology

1 reference

stated in

PubMed Central

reference URL

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retrieved

12 September 2017

Quantification of homozygosity in consanguineous individuals with autosomal recessive disease

1 reference

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PubMed Central

reference URL

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retrieved

12 September 2017

Consanguinity and its relevance to clinical genetics.

1 reference

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PubMed Central

reference URL

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retrieved

12 September 2017

Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0005174

retrieved

21 January 2018

An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19367331

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of consanguinity and its effect on congenital malformation--a hospital based study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19367331

retrieved

12 December 2020

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Identifiers

DOI

10.1371/JOURNAL.PONE.0005174

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ADS bibcode

2009PLoSO...4.5174A

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Fatcat ID

release_zmixsibtefhshpgi34q77i7auu

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ResearchGate publication ID

24278456

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(Q21090070)

The role of inbreeding in the extinction of a European royal dynasty

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