Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1824-7288
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene ; volume:48 ; number:1 ; day:4 ; month:5 ; year:2022 ; pages:1-6 ; date:12.2022
The Italian journal of pediatrics ; 48, Heft 1 (4.5.2022), 1-6, 12.2022
- Creator
-
Serra, Gregorio
Felice, Sofia
Antona, Vincenzo
Pace, Maria Rita Di
Giuffrè, Mario
Piro, Ettore
Corsello, Giovanni
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13052-022-01241-6
- URN
-
urn:nbn:de:101:1-2022071222122766160942
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
2025-08-15T07:26:16+0200
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
- Serra, Gregorio
- Felice, Sofia
- Antona, Vincenzo
- Pace, Maria Rita Di
- Giuffrè, Mario
- Piro, Ettore
- Corsello, Giovanni
- SpringerLink (Online service)
Other Objects (12)
GH successful treatment in a female with a de novo 46,XX,add(X)(p36),t(X;Y)(p36.3;p11.2), growth impairment and SHOX-haploinsufficiency
Atypical and incomplete Kawasaki disease
Genetics and”democracy”
FMF is not always “fever”: from clinical presentation to “treat to target”
Pyridoxine dependent epilepsies: new therapeutical point of view
Concordant Intestinal Atresia in Two Pairs of Monozygotic Twins
Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients
The power of stories in Pediatrics and Genetics
Familial Mediterranean Fever: an unusual cause of liver disease
Kawasaki disease triggered by EBV virus in a child with Familial Mediterranean Fever
Kawasaki disease epidemic: pitfalls
Gambling disorder in adolescents: what do we know about this social problem and its consequences?
GH successful treatment in a female with a de novo 46,XX,add(X)(p36),t(X;Y)(p36.3;p11.2), growth impairment and SHOX-haploinsufficiency
Atypical and incomplete Kawasaki disease
Genetics and”democracy”
FMF is not always “fever”: from clinical presentation to “treat to target”
Pyridoxine dependent epilepsies: new therapeutical point of view
Concordant Intestinal Atresia in Two Pairs of Monozygotic Twins
Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients
The power of stories in Pediatrics and Genetics
Familial Mediterranean Fever: an unusual cause of liver disease
Kawasaki disease triggered by EBV virus in a child with Familial Mediterranean Fever
Kawasaki disease epidemic: pitfalls
Gambling disorder in adolescents: what do we know about this social problem and its consequences?
GH successful treatment in a female with a de novo 46,XX,add(X)(p36),t(X;Y)(p36.3;p11.2), growth impairment and SHOX-haploinsufficiency
Atypical and incomplete Kawasaki disease
Genetics and”democracy”
FMF is not always “fever”: from clinical presentation to “treat to target”
Pyridoxine dependent epilepsies: new therapeutical point of view
Concordant Intestinal Atresia in Two Pairs of Monozygotic Twins
Molecular and phenotypic spectrum of cardio-facio-cutaneous syndrome in Chinese patients
The power of stories in Pediatrics and Genetics
Familial Mediterranean Fever: an unusual cause of liver disease
Kawasaki disease triggered by EBV virus in a child with Familial Mediterranean Fever
Kawasaki disease epidemic: pitfalls