(Q33681952)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

review article

1 reference

title

Pathological features and prenatal diagnosis in the newly recognised limb/pelvis-hypoplasia/aplasia syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

author name string

A Raas-Rothschild

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

R M Goodman

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

S Meyer

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

M B Katznelson

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

S T Winter

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

E Gross

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

M Tamarkin

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

T Ben-Ami

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

L Nebel

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

S Mashiach

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

language of work or name

English

0 references

publication date

1 October 1988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

9 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

volume

25

1 reference

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9 October 2019

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

page(s)

687-697

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

Historical note: the extraordinary handless and footless families of Brazil - 50 years of acheiropodia

9 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051563

A newly recognized genetic syndrome of tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051563

Tetraphocomelia in the syndrome of thrombocytopenia with absent radii (TAR syndrome).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051563

Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051563

The SC phocomelia and the Roberts syndrome: nosologic aspects

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051563

Hypomelia-hypotrichosis-facial hemangioma syndrome (pseudothalidomide, SC syndrome, SC phocomelia syndrome)

21 June 2018

1 reference

12 December 2020

Poly-, syn- and oligodactylyl, aplasia or hypoplasia of fibula, hypoplasia of pelvis and bowing of femora in three sibs--a new autosomal recessive syndrome

1 reference

12 December 2020

Grebe chondrodysplasia and brachydactyly in a family

1 reference

12 December 2020

Syndrome of multiple congenital malformations including phocomelia, thrombocytopenia, encephalocele, and urogenital abnormalities

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.25.10.687

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3066902%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

PubMed publication ID

3066902

1 reference