4.5 Article

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

Related references

Note: Only part of the references are listed.
Review Obstetrics & Gynecology

Reproductive surgery for mullerian anomalies: a review of progress in the last decade

Artur Ludwin et al.

FERTILITY AND STERILITY (2019)

Article Biochemistry & Molecular Biology

Wnt4 coordinates directional cell migration and extension of the Mullerian duct essential for ontogenesis of the female reproductive tract

Renata Prunskaite-Hyyrylainen et al.

HUMAN MOLECULAR GENETICS (2016)

Article Genetics & Heredity

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

Maria Sandbacka et al.

ORPHANET JOURNAL OF RARE DISEASES (2013)

Article Surgery

The ESHRE-ESGE consensus on the classification of female genital tract congenital anomalies

Grigoris F. Grimbizis et al.

GYNECOLOGICAL SURGERY (2013)

Article Obstetrics & Gynecology

Mutations in WNT4 are not responsible for Mullerian duct abnormalities in Chinese women

Xinyue Chang et al.

REPRODUCTIVE BIOMEDICINE ONLINE (2012)

Article Obstetrics & Gynecology

Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Kuster-Hauser syndrome

Susanne Ledig et al.

FERTILITY AND STERILITY (2011)

Review Obstetrics & Gynecology

The history of female genital tract malformation classifications and proposal of an updated system

Pedro Acien et al.

HUMAN REPRODUCTION UPDATE (2011)

Article Genetics & Heredity

SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome

Cristina Gervasini et al.

GENETICS IN MEDICINE (2010)

Article Biochemistry & Molecular Biology

Wnt4/5a signalling coordinates cell adhesion and entry into meiosis during presumptive ovarian follicle development

Florence Naillat et al.

HUMAN MOLECULAR GENETICS (2010)

Article Genetics & Heredity

Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports

Laura Bernardini et al.

ORPHANET JOURNAL OF RARE DISEASES (2009)

Article Genetics & Heredity

Genomic imbalances associated with mullerian aplasia

C. Cheroki et al.

JOURNAL OF MEDICAL GENETICS (2008)

Article Biochemistry & Molecular Biology

Loss of Wnt4 and Foxl2 leads to female-to-male sex reversal extending to germ cells

Chris Ottolenghi et al.

HUMAN MOLECULAR GENETICS (2007)

Article Medicine, General & Internal

A WNT4 mutation associated with Mullerian-duct regression and virilization in a 46,XX woman

A Biason-Lauber et al.

NEW ENGLAND JOURNAL OF MEDICINE (2004)

Article Developmental Biology

Wnt5a is required for proper epithelial-mesenchymal interactions in the uterus

M Mericskay et al.

DEVELOPMENT (2004)

Article Zoology

Wnts and the female reproductive system

M Heikkilä et al.

JOURNAL OF EXPERIMENTAL ZOOLOGY (2001)