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Craniofrontonasal dysplasia
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instance of
scholarly article
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title
Craniofrontonasal dysplasia
(English)
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author name string
I D Young
series ordinal
1
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language of work or name
English
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publication date
April 1987
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published in
Journal of Medical Genetics
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volume
24
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issue
4
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page(s)
193-6
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cites work
Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: a new syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049993
retrieved
29 September 2018
A pedigree possible evidence for the metabolic interference hypothesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049993
retrieved
29 September 2018
Craniofrontonasal dysplasia--a distinct entity with lethality in the male?
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049993
retrieved
29 September 2018
Greig cephalopolysyndactyly: report of 13 affected individuals in three families.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049993
retrieved
29 September 2018
A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049993
retrieved
29 September 2018
Craniofrontonasal dysplasia: clinical and genetic analysis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049993
retrieved
29 September 2018
Frontonasal dysplasia with coronal craniosynostosis in three sibs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049993
retrieved
29 September 2018
Craniosynostosis and syndromes with craniosynostosis: incidence, genetics, penetrance, variability, and new syndrome updating
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049993
retrieved
29 September 2018
Fronto‐facio‐nasal dysostosis – a new autosomal recessive syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3585934
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Radiocephalometric findings in a family with craniofrontonasal dysplasia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/3585934
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.24.4.193
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PMC publication ID
1049993
0 references
PubMed publication ID
3585934
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