Wikidata

(Q43217032)

English

Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype

scientific article published in February 1998

In more languages

Statements

title
Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype (English)
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
author name string
S Gottlieb
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
D A Driscoll
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
H H Punnett
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
B Sellinger
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
B S Emanuel
series ordinal
5
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
M L Budarf
series ordinal
6
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
publication date
1 February 1998
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
volume
62
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
page(s)
495-498
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017
issue
2
1 reference
stated in
Europe PubMed Central
PMCID
1376894
retrieved
16 November 2017

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