- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1755-8166
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Adult expression of a 3q13.31 microdeletion ; volume:7 ; number:1 ; day:20 ; month:3 ; year:2014 ; pages:1-7 ; date:12.2014
Molecular cytogenetics ; 7, Heft 1 (20.3.2014), 1-7, 12.2014
- Urheber
-
Lowther, Chelsea
Costain, Gregory
Melvin, Rebecca
Stavropoulos, Dimitri J.
Lionel, Anath C.
Marshall, Christian R.
Scherer, Stephen W.
Bassett, Anne S.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/1755-8166-7-23
- URN
-
urn:nbn:de:101:1-2021090120574986364288
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:33 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Lowther, Chelsea
- Costain, Gregory
- Melvin, Rebecca
- Stavropoulos, Dimitri J.
- Lionel, Anath C.
- Marshall, Christian R.
- Scherer, Stephen W.
- Bassett, Anne S.
- SpringerLink (Online service)
Ähnliche Objekte (12)
Chromosome 15q24 microdeletion syndrome
16p11.2 microdeletion syndrome: a case report
Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion
The MEF2C -Related and 5q14.3q15 Microdeletion Syndrome
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
NF1 microdeletion syndrome: case report of two new patients
A comprehensive list of human microdeletion and microduplication syndromes
Fetal intracranial hemorrhage in a case of 16p microdeletion
Clinical and molecular characterization of a de novo 19p13.3 microdeletion
Trapping MBD 5 to understand 2q23.1 microdeletion syndrome
Familial inheritance of the 3q29 microdeletion syndrome: case report and review
Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication
Chromosome 15q24 microdeletion syndrome
16p11.2 microdeletion syndrome: a case report
Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion
The MEF2C -Related and 5q14.3q15 Microdeletion Syndrome
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
NF1 microdeletion syndrome: case report of two new patients
A comprehensive list of human microdeletion and microduplication syndromes
Fetal intracranial hemorrhage in a case of 16p microdeletion
Clinical and molecular characterization of a de novo 19p13.3 microdeletion
Trapping MBD 5 to understand 2q23.1 microdeletion syndrome
Familial inheritance of the 3q29 microdeletion syndrome: case report and review
Prenatal phenotypes and pregnancy outcomes of fetuses with 16p11.2 microdeletion/microduplication
Chromosome 15q24 microdeletion syndrome
16p11.2 microdeletion syndrome: a case report
Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion
The MEF2C -Related and 5q14.3q15 Microdeletion Syndrome
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome
NF1 microdeletion syndrome: case report of two new patients
A comprehensive list of human microdeletion and microduplication syndromes
Fetal intracranial hemorrhage in a case of 16p microdeletion
Clinical and molecular characterization of a de novo 19p13.3 microdeletion
Trapping MBD 5 to understand 2q23.1 microdeletion syndrome
Familial inheritance of the 3q29 microdeletion syndrome: case report and review