Robertsonian translocations between chromosomes 13 and 14 (rob [13; 14]) are associated
with some clinical manifestations, including male infertility and recurrent pregnancy loss …

Objective: Rare disease Background: Translocations are the most common type of
chromosomal structural anomalies. In balanced translocations, there is not an obvious loss …

The majority of fluorescence in situ hybridization (FISH) studies on the meiotic segregation
of Robertsonian translocations focus on the most common types, rob (13; 14) and rob (14; …

Background: Robertsonian translocations are structural chromosomal abnormalities caused
by fusion of two acrocentric chromosomes. In carriers of such translocations, different modes …

Robertsonian translocations (ROBs) have an estimated incidence rate of 1/1000 births,
making this type of rearrangement the most common structural chromosomal abnormalities …

Background: Similar rare Robertsonian and balanced reciprocal translocation in both child
and mother with a history of multiple miscarriages in the first trimester was the motive to write …

A Robertsonian Translocation rob (14;15) (q10:q10) in a Patient with Recurrent Abortions: A
Case Report - PMC Back to Top Skip to main content NIH NLM Logo Access keys NCBI …

For genetic counseling of male carriers of chromosomal translocations, the specific
chromosomes and breakpoints involved in the translocation are relevant to know. The …

Robertsonian translocations (RBTs) are associated with an increased risk of aneuploidy.
Single RBT carriers are the most common balanced rearrangements among the carrier …

Background Robertsonian translocations occur in approximately one in every 1000
newborns. Although most Robertsonian translocation carriers are healthy and have a …