- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1752-1947
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Chromosome 3q29 deletion with gastrointestinal malformation: a case report ; volume:5 ; number:1 ; day:5 ; month:7 ; year:2011 ; pages:1-3 ; date:12.2011
Journal of medical case reports ; 5, Heft 1 (5.7.2011), 1-3, 12.2011
- Urheber
-
Masarweh, Ma'in
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/1752-1947-5-285
- URN
-
urn:nbn:de:1111-2016071018919
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:54 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
- Masarweh, Ma'in
- SpringerLink (Online service)
Ähnliche Objekte (12)
Severe growth hormone deficiency and pituitary malformation in a patient with chromosome 2p25 duplication and 2q37 deletion
Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB
Split hand/foot malformation type 1 associated with 7q21.3 deletion - a case report
Jacobsen syndrome: Chromosome deletion at llq23
Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report
Klinefelter syndrome with long-arm X-chromosome deletion
Pancreatic Arteriovenous Malformation Presenting with Upper Gastrointestinal Bleeding: Treatment with Transarterial Embolization—A Case Report
Abernethy malformation: a case report
Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report
Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review
A deletion map of the WAGR region on chromosome II
The butterfly pattern in a patient with chromosome 7 deletion
Severe growth hormone deficiency and pituitary malformation in a patient with chromosome 2p25 duplication and 2q37 deletion
Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB
Split hand/foot malformation type 1 associated with 7q21.3 deletion - a case report
Jacobsen syndrome: Chromosome deletion at llq23
Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report
Klinefelter syndrome with long-arm X-chromosome deletion
Pancreatic Arteriovenous Malformation Presenting with Upper Gastrointestinal Bleeding: Treatment with Transarterial Embolization—A Case Report
Abernethy malformation: a case report
Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report
Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review
A deletion map of the WAGR region on chromosome II
The butterfly pattern in a patient with chromosome 7 deletion
Severe growth hormone deficiency and pituitary malformation in a patient with chromosome 2p25 duplication and 2q37 deletion
Case report of Chromosome 3q25 deletion syndrome or Mucopolysaccharidosis IIIB
Split hand/foot malformation type 1 associated with 7q21.3 deletion - a case report
Jacobsen syndrome: Chromosome deletion at llq23
Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report
Klinefelter syndrome with long-arm X-chromosome deletion
Pancreatic Arteriovenous Malformation Presenting with Upper Gastrointestinal Bleeding: Treatment with Transarterial Embolization—A Case Report
Abernethy malformation: a case report
Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report
Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review
A deletion map of the WAGR region on chromosome II