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English
New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
review article
1 reference
stated in
Europe PubMed Central
title
New multiple congenital anomalies: mental retardation syndrome (MCA/MR) with facio-cutaneous-skeletal involvement
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
main subject
congenital disorder
0 references
author
Renata Rizzo
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
author name string
Borochowitz Z
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
Pavone L
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
Mazor G
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
Dar H
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
publication date
1 July 1992
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
published in
American Journal of Medical Genetics Part A
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
volume
43
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
page(s)
678-685
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
Identifiers
DOI
10.1002/AJMG.1320430405
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
PubMed publication ID
1621757
1 reference
stated in
Europe PubMed Central
PubMed publication ID
1621757
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1621757%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 September 2019
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