Clinical utility gene card for: Mowat-Wilson syndrome

Marcella Zollino; L Garavelli; A. Rauch

doi:10.1038/ejhg.2011.12

Clinical utility gene card for: Mowat-Wilson syndrome

Marcella Zollino, L Garavelli, A. Rauch

Risultato della ricerca: Contributo in rivista › Articolo in rivista › peer review

8 Citazioni (Scopus)

Abstract

N/A

Lingua originale	English
pagine (da-a)	N/A-N/A
Rivista	European Journal of Human Genetics
Volume	19
DOI	https://doi.org/10.1038/ejhg.2011.12
Stato di pubblicazione	Pubblicato - 2011

Keywords

Chromosomes, Human, Pair 2
Facies
Hirschsprung Disease
Homeodomain Proteins
Humans
Intellectual Disability
Microcephaly
Repressor Proteins

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10.1038/ejhg.2011.12

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title = "Clinical utility gene card for: Mowat-Wilson syndrome",

abstract = "N/A",

keywords = "Chromosomes, Human, Pair 2, Facies, Hirschsprung Disease, Homeodomain Proteins, Humans, Intellectual Disability, Microcephaly, Repressor Proteins, Chromosomes, Human, Pair 2, Facies, Hirschsprung Disease, Homeodomain Proteins, Humans, Intellectual Disability, Microcephaly, Repressor Proteins",

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T1 - Clinical utility gene card for: Mowat-Wilson syndrome

AU - Zollino, Marcella

AU - Garavelli, L

AU - Rauch, A.

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KW - Hirschsprung Disease

KW - Homeodomain Proteins

KW - Humans

KW - Intellectual Disability

KW - Microcephaly

KW - Repressor Proteins

KW - Chromosomes, Human, Pair 2

KW - Facies

KW - Hirschsprung Disease

KW - Homeodomain Proteins

KW - Humans

KW - Intellectual Disability

KW - Microcephaly

KW - Repressor Proteins

UR - http://hdl.handle.net/10807/6626

U2 - 10.1038/ejhg.2011.12

DO - 10.1038/ejhg.2011.12

M3 - Article

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JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

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Clinical utility gene card for: Mowat-Wilson syndrome

Abstract

Keywords

OSS delle Nazioni Unite

Accesso al documento

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