C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2 in autism (Q33313519)

25 July 2017

C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2 in autism (English)

1 reference

25 July 2017

0 references

Thayne L Sweeten

1

1 reference

25 July 2017

Daniel W Odell

series ordinal

2

1 reference

25 July 2017

J Dennis Odell

series ordinal

3

1 reference

25 July 2017

Anthony R Torres

series ordinal

4

1 reference

25 July 2017

language of work or name

1 reference

7 January 2008

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25 July 2017

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25 July 2017

9

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25 July 2017

1

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https://scigraph.springernature.com/pub.10.1186/1471-2156-9-1

25 July 2017

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incorrect value

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https://scigraph.springernature.com/pub.10.1186/1471-2350-9-1

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cites work

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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

14 July 2018

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Toward understanding MHC disease associations: partial resequencing of 46 distinct HLA haplotypes

14 July 2018

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Validation and clinical application of a locus-specific polymerase chain reaction- and minisequencing-based assay for congenital adrenal hyperplasia (21-hydroxylase deficiency).

14 July 2018

1 reference

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Complete MHC haplotype sequencing for common disease gene mapping

14 July 2018

1 reference

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The intricate role of complement component C4 in human systemic lupus erythematosus

14 July 2018

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Comprehensive human genome amplification using multiple displacement amplification

14 July 2018

1 reference

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Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease

14 July 2018

1 reference

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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

14 July 2018

1 reference

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Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease as

14 July 2018

1 reference

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Androgenic activity in autism.

14 July 2018

1 reference

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Immunogenetic studies in autism and related disorders

14 July 2018

1 reference

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Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene

14 July 2018

1 reference

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HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation

14 July 2018

1 reference

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Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants

14 July 2018

1 reference

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Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region

14 July 2018

1 reference

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Autism diagnostic interview: a standardized investigator-based instrument.

14 July 2018

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Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

14 July 2018

1 reference

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Increased frequency of the null allele at the complement C4b locus in autism.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2265260

Infantile autism: a genetic study of 21 twin pairs

14 July 2018

1 reference

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Androgens and autistic traits: A study of individuals with congenital adrenal hyperplasia.

14 July 2018

1 reference

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Confirmation of the association of the C4B null allelle in autism.

31 October 2018

1 reference

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Foetal testosterone, social relationships, and restricted interests in children

31 October 2018

1 reference

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Lower cortisol and higher ACTH levels in individuals with autism

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2265260

The transmission disequilibrium test suggests that HLA-DR4 and DR13 are linked to autism spectrum disorder.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2265260

Microconversion betweenCYP21A2andCYP21A1PPromoter Regions Causes the Nonclassical Form of 21-Hydroxylase Deficiency

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2265260

Carrier frequency of congenital adrenal hyperplasia (21-hydroxylase deficiency) in a middle European population

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18179706

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2156-9-1

reason for deprecated rank

incorrect identifier value

1 reference

Dimensions Publication ID

25 July 2017

10.1186/1471-2350-9-1

0 references

1017723004

reason for deprecated rank

incorrect identifier value

0 references

0 references

1 reference

25 July 2017

1 reference