- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1752-1947
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
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
- Creator
-
Masarweh, Ma'in
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/1752-1947-5-285
- URN
-
urn:nbn:de:1111-2016071018919
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
24.10.0008, 1:40 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Masarweh, Ma'in
- SpringerLink (Online service)
Other Objects (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
Abernethy malformation: a case report
Pancreatic Arteriovenous Malformation Presenting with Upper Gastrointestinal Bleeding: Treatment with Transarterial Embolization—A Case Report
Klinefelter syndrome with long-arm X-chromosome deletion
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
Abernethy malformation: a case report
Pancreatic Arteriovenous Malformation Presenting with Upper Gastrointestinal Bleeding: Treatment with Transarterial Embolization—A Case Report
Klinefelter syndrome with long-arm X-chromosome deletion
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
Abernethy malformation: a case report
Pancreatic Arteriovenous Malformation Presenting with Upper Gastrointestinal Bleeding: Treatment with Transarterial Embolization—A Case Report
Klinefelter syndrome with long-arm X-chromosome deletion
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