Twitter | Search | |
Search Refresh
varsome 1h
Novel COL2A1 identified in a newborn with Type 2
Reply Retweet Like
varsome 53m
Rare SMAD9 associated with high bone mass
Reply Retweet Like
Mitch Cruzan 17h
I'm looking for graduate students interested in using genomic approaches to study how somatic mutation accumulation, clonal evolution during vegetative growth, and reproductive processes in plants contribute to standing genetic variation. please rtw.
Reply Retweet Like
MIPAN INDIA Sep 17
Mutation is a process of transferring of title ownership name in records of the revenue department for a property. Contact us-mipan039business@gmail.com
Reply Retweet Like
Raheleh Rahbari Sep 10
After a long review process finally our paper on Similarities & differences in patterns of between mice & humans is out! Congratulations ⁦⁦⁩!
Reply Retweet Like
Island Diva 13h
When you decide to wear polka dots instead of stripes.
Reply Retweet Like
varsome Sep 17
Novel role of PRSS1 implicated in and tumor development
Reply Retweet Like
varsome Sep 11
Case report of a novel BTK in a child With atypical X-Linked agammaglobulinemia and recurrent hemophagocytosis
Reply Retweet Like
BCH Innovation News 13h
Researchers have identified over 100 that can cause specific cancer predisposition syndromes if a is present:
Reply Retweet Like
varsome Sep 17
Gain of function PCSK9 in two unrelated patients with
Reply Retweet Like
Akshayn't Sep 10
Hiroshima Nagasaki born people having 2 extra dicks on biceps
Reply Retweet Like
BadFishPosters Sep 15
Reply Retweet Like
varsome Sep 10
Somatic MEN1 detected in periventricular nodular heterotopia tissue obtained from depth electrodes
Reply Retweet Like
Darcy 🦊 Sep 16
Replying to @slightlyfoxed
While every has been waiting for their letter from Hogwarts, I've always been waiting for mine from Professor Xavier's School for Gifted Youngsters.
Reply Retweet Like
PNAS Sep 10
A in the rhodopsin gene may be responsible for fish species' adaptation to red-shifted light in freshwater or brackish environments, according to a new study whose findings illustrate a remarkable illustration of convergent :
Reply Retweet Like
varsome Sep 12
Novel POU3F4 causes X-linked non-syndromic in a family
Reply Retweet Like
RNA-Seq Blog Sep 13
Using , researchers from were surprised to discover a known as an FLT3 fusion – something that had never before been reported in a pediatric malignancy
Reply Retweet Like
varsome Sep 13
Novel CAPN3 deep intronic as a promising target for therapeutic splice modulation
Reply Retweet Like
Objectif-BD.be Sep 15
Reply Retweet Like
Brightsurf.com Sep 9
linked to flu-related heart complications
Reply Retweet Like