(Q34123574)

English

Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements.

scientific article

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

congenital disorder

0 references

author name string

Elias I Traboulsi

1

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 January 2004

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

Transactions of the American Ophthalmological Society annual meeting

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

102

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

373-389

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

A novel PHOX2A/ARIX mutation in an iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Möbius syndrome redefined: a syndrome of rhombencephalic maldevelopment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Congenital fibrosis syndrome associated with central nervous system abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Mutations of the PAX6 Gene Detected in Patients with a Variety of Optic-Nerve Malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Developmental neurogenetics and neuro-ophthalmology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Okihiro syndrome is caused by SALL4 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Applications of molecular genetics to the understanding of congenital ocular motility disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

CFEOM1, the classic familial form of congenital fibrosis of the extraocular muscles, is genetically heterogeneous but does not result from mutations in ARIX

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Pax6 regulates specification of ventral neurone subtypes in the hindbrain by establishing progenitor domains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

A novel X-linked dominant condition: X-linked congenital isolated ptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Development of noradrenergic neurons in the zebrafish hindbrain requires BMP, FGF8, and the homeodomain protein soulless/Phox2a

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

A second gene for autosomal dominant Möbius syndrome is localized to chromosome 10q, in a Dutch family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Novel dendritic kinesin sorting identified by different process targeting of two related kinesins: KIF21A and KIF21B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Pax-6 is involved in the specification of hindbrain motor neuron subtype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

A gene for isolated congenital ptosis maps to a 3-cM region within 1p32-p34.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Faster sequential genetic linkage computations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome 12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Bilateral Duane's retraction syndrome. A clinical-pathologic case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Duane's retraction syndrome associated with optic nerve hypoplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Congenital ocular fibrosis syndrome associated with the Prader-Willi syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Neural misdirection in congenital ocular fibrosis syndrome: implications and pathogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Joubert's syndrome associated with congenital ocular fibrosis and histidinemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Auditory function in Duane's retraction syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Familial trigeminal anesthesia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Duane's retraction syndrome in the fetal alcohol syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Ocular motility in thalidomide embryopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Oculofacialbulbar palsy in mother and son: review of 26 reports of familial transmission within the 'Möbius spectrum of defects'.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Deletion of chromosome 13 in Moebius syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

The gene for X-linked Kallmann syndrome: a human neuronal migration defect.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Familial Bilateral Optic Nerve Hypoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Three-generation pedigree of a Möbius syndrome variant with chromosome translocation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Generalized fibrosis of the extraocular muscles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Familial Corneal Hypesthesia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

5 July 2018

Classification and surgical management of patients with familial and sporadic forms of congenital fibrosis of the extraocular muscles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

110th ENMC International Workshop: the congenital cranial dysinnervation disorders (CCDDs). Naarden, The Netherlands, 25-27 October, 2002.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Elevation of one eye during tooth brushing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

A patient with de Morsier and Duane syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Control of hindbrain motor neuron differentiation by the homeobox gene Phox2b.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

CFEOM3: a new extraocular congenital fibrosis syndrome that maps to 16q24.2-q24.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Brainstem hypoplasia in the Wildervanck (cervico-oculo-acoustic) syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Absence of the abducens nerve in Duane syndrome verified by magnetic resonance imaging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Effects of prenatal alcohol exposure on the postnatal morphology of the rat oculomotor nucleus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Unilateral Duane's retraction syndrome (Type 1).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Joubert's syndrome, ocular fibrosis, and normal histidine levels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

Congenital fibrosis of the vertically acting extraocular muscles maps to the FEOM3 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1280110

28 October 2018

The molecular basis of the congenital fibrosis syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital Paradoxical Gustatory-Lacrimal Reflex and Lateral Rectus Paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence of genetic heterogeneity in autosomal recessive congenital fibrosis of the extraocular muscles

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Magnetic resonance imaging in Duane's retraction syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Solitary median maxillary central incisor, Duane retraction syndrome, growth hormone deficiency and duplicated thumb phalanx: a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Japanese family with FEOM1-linked congenital fibrosis of the extraocular muscles type 1 associated with spinal canal stenosis and refinement of the FEOM1 critical region

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial congenital facial diplegia: electrophysiologic and genetic studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital oculo-facial paralysis (Moebius syndrome): evidence of dominant inheritance in two families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital fibrosis of the extraocular muscles

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Möbius syndrome. Neuropathologic observations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marcus Gunn jaw winking and Duane's retraction syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital horizontal gaze paralysis and ear dysplasia in a boy with Duane's retraction syndrome and seventh nerve palsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial congenital fourth cranial nerve palsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital unilateral orbital fibrosis with suspected prenatal orbital penetration

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial congenital superior oblique palsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Bilateral Duane syndrome associated with hypogonadotropic hypogonadism and anosmia (Kallmann syndrome)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital unilateral fibrosis, blepharoptosis, and enophthalmos syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of a gene for Möbius syndrome to chromosome 3q by linkage analysis in a Dutch family

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary external ophthalmoplegia synergistic divergence, jaw winking, and oculocutaneous hypopigmentation: a congenital fibrosis syndrome caused by deficient innervation to extraocular muscles

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Möbius syndrome with oculomotor nerve paralysis without abducens paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinically variant fibrosis syndrome in a Turkish family maps to the CFEOM1 locus on chromosome 12

1 reference

https://pubmed.ncbi.nlm.nih.gov/15747768

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15747768%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

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