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Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

2020
journal article
article
10.1093/hmg/ddaa258
Journal
Human Molecular Genetics
140
Author
Martin Ella

Enriquez Annabelle

Sparrow Duncan

Humphreys David

McInerney-Leo Aideen

Leo Paul

Duncan Emma

Iyer Kavitha

Greasby Joelene

Ip Eddie

Giannoulatou Eleni

Sheng Delicia

Wohler Elizabeth

Dimartino Clémantine

Amiel Jeanne

Capri Yline

Lehalle Daphné

Mory Adi

Wilnai Yael

Lebenthal Yael

Gharavi Ali

Krzemień Grażyna

Miklaszewska Monika

Steiner Robert

Raggio Cathy

Blank Robert

Feldman Hagit

Rasouly Hila

Sobreira Nara

Jobling Rebekah

Gordon Christopher

Giampietro Philip

Dunwoodie Sally

Chapman Gavin
Volume
29
Issue
22
Pages
3662-3678
ISSN
0964-6906
eISSN
1460-2083
Language
English
Container language
English
Affiliation
Wydział Lekarski : Instytut Pediatrii
Scopus© citations
15
cris.lastimport.scopus2024-04-07T16:05:22Z
dc.affiliationWydział Lekarski : Instytut Pediatriipl
dc.cm.date2021-03-01
dc.cm.id102403
dc.contributor.authorMartin, Ellapl
dc.contributor.authorEnriquez, Annabellepl
dc.contributor.authorSparrow, Duncanpl
dc.contributor.authorHumphreys, Davidpl
dc.contributor.authorMcInerney-Leo, Aideenpl
dc.contributor.authorLeo, Paulpl
dc.contributor.authorDuncan, Emmapl
dc.contributor.authorIyer, Kavithapl
dc.contributor.authorGreasby, Joelenepl
dc.contributor.authorIp, Eddiepl
dc.contributor.authorGiannoulatou, Elenipl
dc.contributor.authorSheng, Deliciapl
dc.contributor.authorWohler, Elizabethpl
dc.contributor.authorDimartino, Clémantinepl
dc.contributor.authorAmiel, Jeannepl
dc.contributor.authorCapri, Ylinepl
dc.contributor.authorLehalle, Daphnépl
dc.contributor.authorMory, Adipl
dc.contributor.authorWilnai, Yaelpl
dc.contributor.authorLebenthal, Yaelpl
dc.contributor.authorGharavi, Alipl
dc.contributor.authorKrzemień, Grażynapl
dc.contributor.authorMiklaszewska, Monika - 173942 pl
dc.contributor.authorSteiner, Robertpl
dc.contributor.authorRaggio, Cathypl
dc.contributor.authorBlank, Robertpl
dc.contributor.authorFeldman, Hagitpl
dc.contributor.authorRasouly, Hilapl
dc.contributor.authorSobreira, Narapl
dc.contributor.authorJobling, Rebekahpl
dc.contributor.authorGordon, Christopherpl
dc.contributor.authorGiampietro, Philippl
dc.contributor.authorDunwoodie, Sallypl
dc.contributor.authorChapman, Gavinpl
dc.date.accessioned2021-03-01T16:50:27Z
dc.date.available2021-03-01T16:50:27Z
dc.date.issued2020pl
dc.description.number22pl
dc.description.physical3662-3678pl
dc.description.points140
dc.description.volume29pl
dc.identifier.doi10.1093/hmg/ddaa258pl
dc.identifier.eissn1460-2083pl
dc.identifier.issn0964-6906pl
dc.identifier.projectROD UJ / Opl
dc.identifier.urihttps://ruj.uj.edu.pl/xmlui/handle/item/266136
dc.languageengpl
dc.language.containerengpl
dc.rightsDodaję tylko opis bibliograficzny*
dc.rights.licencebez licencji
dc.subtypeArticlepl
dc.titleHeterozygous loss of WBP11 function causes multiple congenital defects in humans and micepl
dc.title.journalHuman Molecular Geneticspl
dc.typeJournalArticlepl
dspace.entity.typePublication
Affiliations
Wydział Lekarski
Miklaszewska, Monika
No affiliation
Martin, Ella
Enriquez, Annabelle
Sparrow, Duncan
Humphreys, David
McInerney-Leo, Aideen
Leo, Paul
Duncan, Emma
Iyer, Kavitha
Greasby, Joelene
Ip, Eddie
Giannoulatou, Eleni
Sheng, Delicia
Wohler, Elizabeth
Dimartino, Clémantine
Amiel, Jeanne
Capri, Yline
Lehalle, Daphné
Mory, Adi
Wilnai, Yael
Lebenthal, Yael
Gharavi, Ali
Krzemień, Grażyna
Steiner, Robert
Raggio, Cathy
Blank, Robert
Feldman, Hagit
Rasouly, Hila
Sobreira, Nara
Jobling, Rebekah
Gordon, Christopher
Giampietro, Philip
Dunwoodie, Sally
Chapman, Gavin

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