AustralieFrV1, Main, Exploration, bibRecordById, pubmed:26228624

Syndrome diagnosis with single-nucleotide polymorphism (SNP) microarray.

Identifieur interne : 001678 ( Main/Exploration ); précédent : 001677; suivant : 001679

Syndrome diagnosis with single-nucleotide polymorphism (SNP) microarray.

Auteurs : Matthew Edwards [Australie] ; Sally Brescianini [Australie] ; Catherine Allgood [Australie] ; Michael Freelander [Australie] ; Richard Dunstan [Australie] ; Patrick Patradoon-Ho [Australie] ; Raymond Chin [Australie] ; Lucy Morgan [Australie] ; Tasnuba Pervez [Australie] ; Marie Legendre [France] ; Trent Burgess [Australie] ; Serge Amselem [France] ; John Whitehall [Australie]

Source :

Journal of paediatrics and child health [ 1440-1754 ] ; 2016.

RBID : pubmed:26228624

Descripteurs français

KwdFr :
- Analyse sur microréseau, Dépistage génétique, Enfant d'âge préscolaire, Humains, Mâle, Nouveau-né, Polymorphisme de nucléotide simple, Syndrome, Troubles de la motilité ciliaire (diagnostic).
MESH :
- diagnostic : Troubles de la motilité ciliaire.
- Analyse sur microréseau, Dépistage génétique, Enfant d'âge préscolaire, Humains, Mâle, Nouveau-né, Polymorphisme de nucléotide simple, Syndrome.

English descriptors

KwdEn :
- Child, Preschool, Ciliary Motility Disorders (diagnosis), Genetic Testing, Humans, Infant, Newborn, Male, Microarray Analysis, Polymorphism, Single Nucleotide, Syndrome.
MESH :
- diagnosis : Ciliary Motility Disorders.
- Child, Preschool, Genetic Testing, Humans, Infant, Newborn, Male, Microarray Analysis, Polymorphism, Single Nucleotide, Syndrome.

DOI: 10.1111/jpc.12981
PubMed: 26228624

Affiliations:

Le document en format XML

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<author><name sortKey="Pervez, Tasnuba" sort="Pervez, Tasnuba" uniqKey="Pervez T" first="Tasnuba" last="Pervez">Tasnuba Pervez</name>
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<author><name sortKey="Legendre, Marie" sort="Legendre, Marie" uniqKey="Legendre M" first="Marie" last="Legendre">Marie Legendre</name>
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<term>Genetic Testing</term>
<term>Humans</term>
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<keywords scheme="MESH" xml:lang="fr"><term>Analyse sur microréseau</term>
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<term>Enfant d'âge préscolaire</term>
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<name sortKey="Chin, Raymond" sort="Chin, Raymond" uniqKey="Chin R" first="Raymond" last="Chin">Raymond Chin</name>
<name sortKey="Dunstan, Richard" sort="Dunstan, Richard" uniqKey="Dunstan R" first="Richard" last="Dunstan">Richard Dunstan</name>
<name sortKey="Freelander, Michael" sort="Freelander, Michael" uniqKey="Freelander M" first="Michael" last="Freelander">Michael Freelander</name>
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<name sortKey="Patradoon Ho, Patrick" sort="Patradoon Ho, Patrick" uniqKey="Patradoon Ho P" first="Patrick" last="Patradoon-Ho">Patrick Patradoon-Ho</name>
<name sortKey="Pervez, Tasnuba" sort="Pervez, Tasnuba" uniqKey="Pervez T" first="Tasnuba" last="Pervez">Tasnuba Pervez</name>
<name sortKey="Whitehall, John" sort="Whitehall, John" uniqKey="Whitehall J" first="John" last="Whitehall">John Whitehall</name>
</country>
<country name="France"><region name="Île-de-France"><name sortKey="Legendre, Marie" sort="Legendre, Marie" uniqKey="Legendre M" first="Marie" last="Legendre">Marie Legendre</name>
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Serveur d'exploration sur les relations entre la France et l'Australie

Syndrome diagnosis with single-nucleotide polymorphism (SNP) microarray.

Syndrome diagnosis with single-nucleotide polymorphism (SNP) microarray.

Source :

Descripteurs français

English descriptors

Links toward previous steps (curation, corpus...)

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	Serveur d'exploration sur les relations entre la France et l'Australie
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