(Q33680876)

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Meckel syndrome

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

Europe PubMed Central

Meckel syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Salonen R

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Paavola P

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 June 1998

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

35

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

497-501

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Genetic heterogeneity of Meckel syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Associated malformations in the family of a patient with Meckel syndrome: heterozygous expression?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

The Meckel syndrome: report of two Japanese sibs and a review of literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Meckel syndrome: what are the minimum diagnostic criteria?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Polydactyly in a carrier of the gene for the Meckel syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Dandy-Walker malformation in the Meckel syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Ultrasonographic parameters in the prenatal diagnosis of Meckel syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

The Meckel syndrome: clinicopathological findings in 67 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Meckel syndrome in different populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Arhinencephaly, encephalocele, and 13-15 trisomy syndrome with normal chromosomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Polycystic kidneys associated with malformations of the brain, polydactyly, and other birth defects in newborn sibs. A lethal syndrome showing the autosomal-recessive pattern of inheritance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Genetics of the Meckel syndrome (dysencephalia splanchnocystica)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Encephalocele, polycystic kidneys, and polydactyly as an autosomal recessive trait simulating certain other disorders: the Meckel syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

The Meckel syndrome with limited expression in relatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Ocular Manifestations of the Meckel Syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

High incidence of Meckel's syndrome in Gujarati Indians

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brain pathology in the Meckel syndrome: a study of 59 cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Pathology of renal and hepatic anomalies in Meckel syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

A distinctive triad of malformations of the central nervous system in the Meckel-Gruber syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

The cerebro-reno-digital syndromes: a new community

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Meckel syndrome and neural tube defects in Kuwait

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Meckel's syndrome: an unusual pedigree

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

21 June 2018

Goldston syndrome reconsidered.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

30 October 2018

Relatively high prevalence of the Meckel syndrome among Jews

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

30 October 2018

Cystic dysplastic kidneys associated with Dandy-Walker malformation and congenital hepatic fibrosis. Report of two cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051345

30 October 2018

Dandy-Walker malformation in the Meckel syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survival in an infant with a prenatally diagnosed Meckel syndrome variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meckel syndrome and Dandy Walker malformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of the Meckel-Gruber syndrome at eleven to fourteen weeks' gestation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic heterogeneity in Meckel syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polycystic kidneys and liver in two siblings with other severe congenital abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Meckel's syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly"

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal morphology in Meckel's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Meckel Syndrome. Pathological and cytogenetic observations in eight cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Survival and spectrum of anomalies in the Meckel syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Meckel syndrome in Finland: epidemiologic and genetic aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visceral anomalies in the Meckel syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meckel-Gruber syndrome. Importance of prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dandy-Walker malformation (variant), cystic dysplastic kidneys, and hepatic fibrosis: a distinct entity or Meckel syndrome?

1 reference

https://pubmed.ncbi.nlm.nih.gov/9643292

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.35.6.497

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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