Konferenzschrift | Kongress
Prader-Willi syndrome and other chromosome 15q deletion disorders : [proceedings of the NATO Advanced Research Workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders held at Noordwijkerhout (The Netherlands) from May 2 - 3, 1991]
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISBN
-
9783540530954
3540530959
9780387530956
0387530959
- Dimensions
-
25 cm
- Extent
-
XII, 265 S.
- Language
-
Deutsch
- Notes
-
Ill., graph. Darst.
Literaturangaben
- Bibliographic citation
-
NATO ASI series / H / NATO ; Vol. 61, Series H, Cell biology
- Keyword
-
Prader-Willi-Syndrom
Chromosomenanomalie
Angelman-Syndrom
- Event
-
Veröffentlichung
- (where)
-
Berlin, Heidelberg, New York, London, Paris, Tokyo, Hong Kong, Barcelona, Budapest
- (who)
-
Springer
- (when)
-
1992
- Contributor
-
Cassidy, Suzanne B.
Advanced Research Workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders (1991 : Noordwijkerhout)
- Table of contents
- Rights
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
-
11.06.2025, 1:38 PM CEST
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.
Object type
- Konferenzschrift
- Kongress
Associated
- Cassidy, Suzanne B.
- Advanced Research Workshop on Prader-Willi Syndrome and Other Chromosome 15q Deletion Disorders (1991 : Noordwijkerhout)
- Springer
Time of origin
- 1992
Other Objects (12)
Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome
Management of Prader-Willi syndrome
Management of Prader-Willi syndrome
Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q
Prader-Willi syndrome : selected research and management issues
A homozygous deletion of exon 5 of KYNU resulting from a maternal chromosome 2 isodisomy (UPD2) causes Catel-Manzke-Syndrome/VCRL syndrome
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome
Somatische Mosaike und atypische Deletionen bei Patienten mit Prader-Willi- und Angelman-Syndrom
A deletion map of the WAGR region on chromosome II
Prader, G.
Prader-Willi-Syndrome : effects of of human growth hormone treatment ; 11 tables
Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome
Management of Prader-Willi syndrome
Management of Prader-Willi syndrome
Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q
Prader-Willi syndrome : selected research and management issues
A homozygous deletion of exon 5 of KYNU resulting from a maternal chromosome 2 isodisomy (UPD2) causes Catel-Manzke-Syndrome/VCRL syndrome
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome
Somatische Mosaike und atypische Deletionen bei Patienten mit Prader-Willi- und Angelman-Syndrom
A deletion map of the WAGR region on chromosome II
Prader, G.
Prader-Willi-Syndrome : effects of of human growth hormone treatment ; 11 tables
Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome
Management of Prader-Willi syndrome
Management of Prader-Willi syndrome
Impact of PPM1D mutations in patients with myelodysplastic syndrome and deletion of chromosome 5q
Prader-Willi syndrome : selected research and management issues
A homozygous deletion of exon 5 of KYNU resulting from a maternal chromosome 2 isodisomy (UPD2) causes Catel-Manzke-Syndrome/VCRL syndrome
Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome
Somatische Mosaike und atypische Deletionen bei Patienten mit Prader-Willi- und Angelman-Syndrom
A deletion map of the WAGR region on chromosome II
Prader, G.