Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia

zu Verbundenen Objekten

Standort
Deutsche Nationalbibliothek Frankfurt am Main
ISSN
1755-8166
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
online resource.

Erschienen in
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

Schlagwort
Erbkrankheit
Erbschaden

Urheber
Demir Eksi, Durkadin
Beteiligte Personen und Organisationen
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
10.1186/s13039-018-0359-3
URN
urn:nbn:de:1111-201803305252
Rechteinformation
Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:48 MESZ

Datenpartner

Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Original beim Datenpartner anzeigen

Beteiligte

  • 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)

Ähnliche Objekte (12)

Evaluation of SHOX copy number variations in patients with Müllerian aplasia

Evaluation of SHOX copy number variations in patients with Müllerian aplasia

TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia

TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia

Anti-Müllerian hormone independently affect mtDNA copy number in human granulosa cells

Anti-Müllerian hormone independently affect mtDNA copy number in human granulosa cells

High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia

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

Analysis of copy number variations of WNT4 gene in a Chinese population with Müllerian anomalies

Finding regions of aberrant DNA copy number associated with tumor phenotype

Hochschulschrift

Finding regions of aberrant DNA copy number associated with tumor phenotype

Identification of recurrent regions of copy-number variants across multiple individuals

Identification of recurrent regions of copy-number variants across multiple individuals

Tandem repeat copy-number variation in protein-coding regions of human genes

Tandem repeat copy-number variation in protein-coding regions of human genes

Protein-altering variants at copy number-variable regions influence diverse human phenotypes

Protein-altering variants at copy number-variable regions influence diverse human phenotypes

Copy-number-variation and copy-number-alteration region detection by cumulative plots

Copy-number-variation and copy-number-alteration region detection by cumulative plots

Copy number variation and disease

Aufsatzsammlung

Copy number variation and disease

Copy number variations and stroke

Copy number variations and stroke

Verbundene Objekte