Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8166
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia ; volume:11 ; number:1 ; day:3 ; month:2 ; year:2018 ; pages:1-8 ; date:12.2018
Molecular cytogenetics ; 11, Heft 1 (3.2.2018), 1-8, 12.2018
- Keyword
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Erbkrankheit
Erbschaden
- Creator
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Demir Eksi, Durkadin
- Contributor
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Shen, Yiping
Erman, Munire
Chorich, Lynn P.
Sullivan, Megan E.
Bilekdemir, Meric
Yılmaz, Elanur
Luleci, Guven
Kim, Hyung-Goo
Alper, Ozgul M.
Layman, Lawrence C.
SpringerLink (Online service)
- DOI
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10.1186/s13039-018-0359-3
- URN
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urn:nbn:de:1111-201803305252
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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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
- Demir Eksi, Durkadin
- Shen, Yiping
- Erman, Munire
- Chorich, Lynn P.
- Sullivan, Megan E.
- Bilekdemir, Meric
- Yılmaz, Elanur
- Luleci, Guven
- Kim, Hyung-Goo
- Alper, Ozgul M.
- Layman, Lawrence C.
- SpringerLink (Online service)
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Evaluation of SHOX copy number variations in patients with Müllerian aplasia
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Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies
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Evaluation of SHOX copy number variations in patients with Müllerian aplasia
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High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia
Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies
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Identification of recurrent regions of copy-number variants across multiple individuals
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Protein-altering variants at copy number-variable regions influence diverse human phenotypes
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