| Original language | English |
|---|---|
| Pages (from-to) | 543-547 |
| Number of pages | 5 |
| Journal | Journal of Medical Genetics |
| Volume | 37 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - 1 Jul 2000 |
| Externally published | Yes |
Cite this
}
Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation. / Boyne, J.; Evans, Steve; Pollitt, Rodney J.; Taylor, Christopher J.; Dalton, Ann.
In: Journal of Medical Genetics, Vol. 37, No. 7, 01.07.2000, p. 543-547.Research output: Contribution to journal › Letter
TY - JOUR
T1 - Many ΔF508 heterozygote neonates with transient hypertrypsinaemia have a second, mild CFTR mutation
AU - Boyne, J.
AU - Evans, Steve
AU - Pollitt, Rodney J.
AU - Taylor, Christopher J.
AU - Dalton, Ann
PY - 2000/7/1
Y1 - 2000/7/1
UR - http://www.scopus.com/inward/record.url?scp=0033624507&partnerID=8YFLogxK
U2 - 10.1136/jmg.37.7.543
DO - 10.1136/jmg.37.7.543
M3 - Letter
C2 - 10970190
AN - SCOPUS:0033624507
VL - 37
SP - 543
EP - 547
JO - Journal of Medical Genetics
JF - Journal of Medical Genetics
SN - 0022-2593
IS - 7
ER -