- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Proximal Deletion 12q with a New Insight to Growth Retardation ; volume:11 ; number:3 ; year:2020 ; pages:115-124
Molecular syndromology ; 11, Heft 3 (2020), 115-124
- Creator
-
Sobol, Maria
Thuresson, Ann-Charlotte
Palmberg, Nathalie
Soussi Zander, Cecilia
- DOI
-
10.1159/000507410
- URN
-
urn:nbn:de:101:1-2020071600344979784816
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:48 AM 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.
Associated
- Sobol, Maria
- Thuresson, Ann-Charlotte
- Palmberg, Nathalie
- Soussi Zander, Cecilia
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Intrauterine growth retardation
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Intrauterine growth retardation - small events, big consequences
Prenatal diagnosis and treatment of intrauterine growth retardation
Ultrasound and biochemical findings in intrauterine growth retardation
Intrauterine growth retardation (IUGR) in pre-term infants
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Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay
Unified Growth Theory: an insight
1q25.2-q31.3 Deletion in a female with mental retardation, clinodactyly, minor facial anomalies but no growth retardation
Intrauterine growth retardation
Psychomotor retardation with a 1q42.11–q42.12 deletion
Intrauterine growth retardation - small events, big consequences
Prenatal diagnosis and treatment of intrauterine growth retardation
Ultrasound and biochemical findings in intrauterine growth retardation
Intrauterine growth retardation (IUGR) in pre-term infants
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Technological Retardation
Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?
Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay