Identification of genetic causes in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a systematic review of the literature

VE Triantafyllidi, D Mavrogianni, A Kalampalikis… - Children, 2022 - mdpi.com
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a congenital condition characterizing
females with absence of the uterus and part of the vagina. Several genetic defects have …

Molecular basis of müllerian agenesis causing congenital uterine factor infertility—a systematic review

R Dube, SS Kar, M Jhancy, BT George - International Journal of …, 2023 - mdpi.com
Infertility affects around 1 in 5 couples in the world. Congenital absence of the uterus results
in absolute infertility in females. Müllerian agenesis is the nondevelopment of the uterus …

Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes–Brocks syndrome 2

A Christians, E Kesdiren, I Hennies, A Hofmann… - Human Genetics, 2023 - Springer
Most patients with congenital anomalies of the kidney and urinary tract (CAKUT) remain
genetically unexplained. In search of novel genes associated with CAKUT in humans, we …

Expression patterns of some follicular genes and their association with fertility trait in goat.

OE Othman, NAA El-Maaty - 2023 - cabidigitallibrary.org
The aim of this study was to assess the expression of some follicular genes and their
association with fertility trait in goat using Qt-PCR. Two groups of Zaraibi goat breed; high …

[PDF][PDF] Study of mullerian duct anomalies using magnetic resonance imaging technique in a tertiary care hospital of Assam

D Bhuyan, PR Choudhury, P Agarwala… - Indian J Clin Anat …, 2016 - academia.edu
Background: Mullerian duct anomalies (MDA) consist of a set of structural malformations
resulting from abnormal development of the paramesonephric or Mullerian ducts. Mullerian …