- DNA guilds? What is that?
- DNA Guilds Introduction
- L206w
- Top TEN MUTATIONS ON OUR SITE
- DNA sequencing what company does this?
- Top 20 Mutation on our site
- Top 30 Mutation on our site
- 2585delT
- Can companies patent your genes?
- Is there anyone like me?
- F1052V - Question about Pipeline drug classification
- Delta F508 & G542X
- F508del/M952T
- Test Result
- 1584g>a
- Please help me understand
- Ambry Amplified testing????
- Getting ready for the deluge of genetic info!
- DeltaF508 and E60x?
- 105 additional genetic markers that cause CF pinpointed
- My son has not one, but two very rare mutations
- DF508/i507del I have just been thrown off phase 3 combo trial.
- scientists pinpoint 105 genetic errors that cause CF.
- Can anyone explain these genes?
- Please help me understand daughters mutations
- Kalydeco gets approval for eight more mutations
- "Roadmap to a Cure"
- 4 month old exhibiting pulmonary CF symptoms, R117H and DeltaF508
- Another interesting clinical trial to correct F508del-CFTR
- 2 little CF warriors
- Addition of VX-661 to KALYDECO(R) (ivacaftor) Improves Lung Function short study P2
- R75x ?
- F508 Delta and R117H .... CFRMS or Cystic Fibrosis Related Metabolic Syndrome
- Gene confusion R117H/5T
- Kalydeco New Drug Application submited to FDA for R117H for 18 yo and older
- G542X but I have CBAVD
- Anyone with DF508/R1162L
- F508 & d110h
- Still looking for others with 124del23bp
- C.777delT & DF508
- Newborn has 2 mutations-I1366T & DelF508..HELP?
- F508 and M265R
- Kalydeco With "Other" Mutations
- F508 and I148T/possible CF symptoms?
- 1 copy F508del mutation
- Need someone who did full-genetic sequencing in 2005 or earlier
- Homozygous for D508, PI but...
- S945l
- Desperately looking for others with delta f508 and s1235r
- Help with Prescription for Kalydeco off-label
- R297Q /30 years old
- 502 bad gateway
- two copies of m470v (not one but two copies)
- DNA results
- i1366T
- Sweat Test after CFTR Test Negative
- 124del23bp aka c.-9_14del23 anybody out there?
- 1471delA and DeltaF508
- Test For The "Normal' CFTR Gene?
- Mutation Database
- question on mutatuon
- How to find out classifications for Mutation D36N.
- More Promising News
- Even More Promising News!
- Delta 508 & C2657+2_2657+3INSA
- More than 2 mutations?
- positive sweat test but no cf ???
- Question on residual function
- g1069r
- referral for CFTR
- I am not going to sit back anymore.
- 2183aa > G or S945L
- DeltaF508 c.1584G>A
- Hi All. Throwing this out there to see if anyone can help. Still no CF diagnoise.
- D579g
- DeltaF508 and c1521_1523 Deletion CTT. Please help!!!
- P.arg75.gln
- anyone have DeltaF508and p.Leu467pro
- Fibrosis vest for sale
- G1244E and DF508
- Gene f508 and r117h ~7t
- Delta F508 + D797A
- Looking for a little more information.
- R117h + ivs8-5t/78/9t/7t
- CFTR nonsense w-1204, nonsense w-1143
- gene c.3140-26a
- Which is the best Ambry Genzyme quest or someone else?
- ATP-sulfurylase for research use
- Anyone with Mutation 3849+10kbC-T
- Advice needed
- dF508 and Sweat Test experience....
- Df508 & m470v / 5t / 12tg
- need to understand
- trying to understand if I have cystic fibrosis
- Can someone explain in plain English
- Curious about thoughts on these mutations
- Anyone have any insight into these findings?
- Anyone have this combination?
- F508 and I148T
- Great news
- Newbie with Lots of Questions
- My son has this combination: 3849+10kbC and 712-G->T
- unknown genotype
- Trouble understanding test R117h hetero or homo...
- Companies are Stealing Genetic/ Genomic Data. Are they Stealing Yours? Take a Survey
- Premie twin with w1089x with Variant TG12-5T/TG11-7T
- uncommon variant, what to do- need advice? 3849+10kbC->T and 5T
- Starting to think I may actually have CF....
- 2585delT
- Question on L183i also known as the c.547C>A - Cystic Fibrosis mutation
- S1235R mutation
- Starting Symdeko
- ΔF508 and R334Q
- Anyone with 1585-1G>A or 3140-26A>G? Uncommon variant
- C.2657+5g>a and p.thr164ala Varient of uncertain significance
- C.743+2T>C p? (Legacy name 875+2T>C)
- I could really use some help understanding
- Classic CF class 1 and 2 mutations, no symptoms
- Help explaining?
- f508 and 5T - looking for CRMS experiences
- D110H Mutation
- 4016insT Mutation?
- Trikafta eligibility
- Cystic Fibrosis research project
- Best online dissertation assistance In The UK