- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1752-1947
- Extent
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Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report ; volume:8 ; number:1 ; day:9 ; month:10 ; year:2014 ; pages:1-5 ; date:12.2014
Journal of medical case reports ; 8, Heft 1 (9.10.2014), 1-5, 12.2014
- Creator
-
Ponti, Giovanni
- Contributor
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Pellacani, Giovanni
Tomasi, Aldo
Percesepe, Antonio
Guarneri, Carmelo
Guerra, Azzurra
Mandel, Victor Desmond
Kisla, Elif
Cevikel, Piril
Neri, Claudia
Menozzi, Cristina
Seidenari, Stefania
SpringerLink (Online service)
- DOI
-
10.1186/1752-1947-8-333
- URN
-
urn:nbn:de:1111-201607116408
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:52 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
- Ponti, Giovanni
- Pellacani, Giovanni
- Tomasi, Aldo
- Percesepe, Antonio
- Guarneri, Carmelo
- Guerra, Azzurra
- Mandel, Victor Desmond
- Kisla, Elif
- Cevikel, Piril
- Neri, Claudia
- Menozzi, Cristina
- Seidenari, Stefania
- SpringerLink (Online service)
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Outcomes of pregnancies with trisomy 16 mosaicism detected by NIPT: a series of case reports
Two cases of placental trisomy 21 mosaicism causing false-negative NIPT results
A case of placental trisomy 18 mosaicism causing a false negative NIPT result
The significance of trisomy 7 mosaicism in noninvasive prenatal screening
Mosaicism trisomy 10 in a 14-month-old child with additional neurological abnormalities: case report and literature review
Heterotopic ossification after patellar tendon repair in a man with trisomy 8 mosaicism: a case report and literature review
Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening
Partial and complete trisomy 14 mosaicism: clinical follow-up, cytogenetic and molecular analysis
Noninvasive prenatal testing for fetal trisomy 9 mosaicism by maternal plasma DNA sequencing
Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review
Trisomy 5p with bilateral congenital diaphragmatic hernia: a case report
Prenatal diagnosis of a trisomy 7/trisomy 13 mosaicism
Outcomes of pregnancies with trisomy 16 mosaicism detected by NIPT: a series of case reports
Two cases of placental trisomy 21 mosaicism causing false-negative NIPT results
A case of placental trisomy 18 mosaicism causing a false negative NIPT result
The significance of trisomy 7 mosaicism in noninvasive prenatal screening
Mosaicism trisomy 10 in a 14-month-old child with additional neurological abnormalities: case report and literature review
Heterotopic ossification after patellar tendon repair in a man with trisomy 8 mosaicism: a case report and literature review
Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening
Partial and complete trisomy 14 mosaicism: clinical follow-up, cytogenetic and molecular analysis
Noninvasive prenatal testing for fetal trisomy 9 mosaicism by maternal plasma DNA sequencing
Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review