(Q34805442)

English

Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes

scientific article

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scholarly article

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes (English)

1 reference

Europe PubMed Central

4 August 2017

Fraser syndrome

1 reference

based on heuristic

inferred from title

author name string

Slavotinek AM

1

1 reference

Europe PubMed Central

4 August 2017

Tifft CJ

2

1 reference

Europe PubMed Central

4 August 2017

language of work or name

0 references

publication date

1 September 2002

1 reference

Europe PubMed Central

4 August 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

4 August 2017

39

1 reference

Europe PubMed Central

4 August 2017

623-633

1 reference

Europe PubMed Central

4 August 2017

9

1 reference

Europe PubMed Central

4 August 2017

'Hard' and 'soft' principles defining the structure, function and regulation of keratin intermediate filaments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Modifier genes and variation in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Prenatal detection of Fraser syndrome without cryptophthalmos: case report and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fraser-cryptophthalmos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Microblepharon: a case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Two sibs with microcephaly, hygroma colli, renal dysplasia, and cutaneous syndactyly: a new lethal MCA syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Surgical correction for complete cryptophthalmos: case report and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Syndromic and isolated cryptophthalmos.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

MURCS association: case report and review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Rehabilitation of a child with partial unilateral cryptophthalmos and multiple congenital anomalies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fraser syndrome (cryptophthalmos [hidden eye]-syndactyly syndrome).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Resynthesizing evolutionary and developmental biology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fraser syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Pulmonary hyperplasia in the Fraser cryptophthalmos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fraser syndrome: a case report and review of the otolaryngologic manifestations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Bilateral and unilateral mesodermal corneal metaplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Cryptophthalmos syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fraser syndrome presenting as monozygotic twins with bilateral renal agenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

ENT abnormalities associated with Fraser syndrome: case report and literature review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

The clinical spectrum of the Fraser syndrome: report of three new cases and review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Isolated and syndromic cryptophthalmos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Cryptophthalmos--syndactyly syndrome without cryptophthalmos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Cryptophthalmos: surgical treatment of the congenital symblepharon variant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fraser syndrome (cryptophthalmos-syndactyly syndrome): a review of eleven cases with postmortem findings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Congenital corneal anaesthesia and the MURCS association: a case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Orbito-palpebral reconstruction in 2 cases of partial cryptophthalmos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fraser syndrome with renal agenesis in two consanguineous Turkish families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

[Cryptophthalmos solum corneae]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Abortive cryptophthalmos: a case report and a review of cryptophthalmos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

New observations on midline defects: coincidence of anophthalmos, microphthalmos and cryptophthalmos with hypothalamic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fused eyelids, airway anomalies, ovarian cysts, and digital abnormalities in siblings: a new autosomal recessive syndrome or a variant of Fraser syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Eyelid and fornix reconstruction in bilateral abortive cryptophthalmos (Fraser syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Ablepheron macrostomia syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

8 July 2018

Fraser syndrome: diagnosed in a 50-year-old museum specimen.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

[Apropos of a case of incomplete cryptophthalmos]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Congenital symblepharon (abortive cryptophthalmos) associated with meningoencephalocele.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Anaesthetic considerations in a patient with Fraser syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Syndrome malformatif avec cryptophtalmie

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Heterotopic smooth muscle in the choroid of two patients with cryptophthalmos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Expressivity of familial forms of Fraser syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Fraser syndrome (cryptophthalmos with syndactyly) in the fetus and newborn.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Fraser syndrome with bladder pseudoexstrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Cryptophthalmos, dental and oral abnormalities, and brachymesophalangy of second toes: new syndrome or Fraser syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Laryngeal atresia presenting as fetal ascites, olygohydramnios and lung appearance mimicking cystic adenomatoid malformation in a 25-week-old fetus with Fraser syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Fraser syndrome associated with anterior urethral atresia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Surgical correction of incomplete cryptophthalmos in Fraser syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Diagnostic echographic findings in cryptophthalmos syndrome (Fraser syndrome)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

[Anesthetic management of a patient with a cryptophthalmos syndactyly syndrome and subglottic stenosis]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Sclerocornea, hypertelorism, syndactyly, and ambiguous genitalia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Fraser (Cryptophthalmos-syndactyly) syndrome: a case with bilateral anophthalmia but presence of normal eyelids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Fraser syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Renal agenesis as a diagnostic feature of the crypthophthalmos-syndactyly syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Cryptophthalmos Syndrome with Bilateral Renal Agenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Cryptophthalmos syndrome. Clinical and histopathological findings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Prenatal diagnosis of Fraser syndrome at 18.5 weeks gestation, with autopsy findings at 19 weeks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Case report: Fraser syndrome, cryptophthalmos with small bowel malrotation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Fraser syndrome. Cryptophthalmos syndactyly syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

Fraser's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735240

26 October 2018

ENT manifestations of Fraser syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New familial syndrome of unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies in Manitoba Indians

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete cryptophthalmos: case report with normal flash-VEP and ERG

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unilateral cryptophthalmos

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cryptophthalmos syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epidemiological study of congenital diaphragmatic defects with special reference to aetiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulmonary hyperplasia in Fraser syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral renal agenesis and cytomegalovirus infection in a case of Fraser syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Bilateral complete cryptophthalmos. Illustration with a case. Review of the literature]

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lenz microphthalmia: a malformation syndrome with variable expression of multiple congenital anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microphthalmia--prenatal ultrasonic diagnosis: a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral cryptophthalmos with multiple associated congenital malformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gonadal dysgenesis and gonadoblastoma in situ in a female with Fraser (cryptophthalmos) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Bilateral complete cryptophthalmos]

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal lung growth in congenital laryngeal atresia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Symmetrical partial lateral 'cryptophthalmos'. A new concept of its embryological pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Syndromic cryptophthalmos

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fraser syndrome: prenatal ultrasonic detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal echogenic lung lesions: prenatal ultrasound diagnosis and outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surgical reconstruction in cryptophthalmos

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bilateral abortive cryptophthalmos associated with oculocutaneous albinism

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Description of palpebral involvement in Fraser's syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rokitansky syndrome and MURCS association--clinical features and basis for diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cryptophthalmos

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant modifier DFNM1 suppresses recessive deafness DFNB26

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal agenesis and the Fraser syndrome: 4 observations

1 reference

https://pubmed.ncbi.nlm.nih.gov/12205104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.39.9.623

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

1 reference

Europe PubMed Central

4 August 2017

ResearchGate publication ID

0 references

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