(Q72550835)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6132872%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

The Meckel Syndrome. Pathological and cytogenetic observations in eight cases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6132872%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

author name string

P Moerman

1

1 reference

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27 October 2019

E Verbeken

2

1 reference

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27 October 2019

J P Fryns

3

1 reference

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27 October 2019

P Goddeeris

4

1 reference

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27 October 2019

J M Lauweryns

5

1 reference

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27 October 2019

publication date

1 January 1982

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27 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6132872%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

volume

62

1 reference

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27 October 2019

page(s)

240-245

1 reference

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27 October 2019

issue

3

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00333528

27 October 2019

exact match

0 references

cites work

[Three new cases of Meckel's syndrome or Gruber's splanchnocystic dysencephaly in siblings. Anatomo-pathologic and cytogenetic study. Nosologic discussion]

1 reference

12 December 2020

A casuistic report on the Gruber or Meckel syndrome

1 reference

12 December 2020

The ductal plate malformation

1 reference

12 December 2020

Oral-facial-digital syndrome, with polycystic kidneys and liver: pathological and cytogenetic studies

1 reference

12 December 2020

Genetics of the Meckel syndrome (dysencephalia splanchnocystica)

1 reference

12 December 2020

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

1 reference

12 December 2020

Etiologic Heterogeneity of Neural-Tube Defects

1 reference

12 December 2020

The Meckel syndrome with limited expression in relatives

1 reference

12 December 2020

[Meckel syndrome. Difficulties in prenatal diagnosis caused by variability of expression (observations on two families)]

1 reference

12 December 2020

A Meckel-like syndrome?

1 reference

12 December 2020

Meckel's syndrome (dysencephalia splanchno-cystica) in two Pakistani sibs

1 reference

12 December 2020

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

12 December 2020

Polycystic kidneys, internal hydrocephalus and polydactylism in newborn siblings

1 reference

12 December 2020

Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00333528

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6132872%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1 reference