A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome) (Q28278792)
scientific article
Language:
(P31) (Q13442814)
(P50) (Q43097735)
(P304) 445-7
(P407) (Q1860)
(P433) 4
(P478) 12
(P577) +1996-04-00T00:00:00Z
(P921) (Q104053)
(Q114049690)
(P1433) (Q976454)
(P1476) "A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)" (language: en)
(P2093) J Osinga
G Tan-Sindhunata
Y Wu
E J Kamsteeg
R P Stulp
C van Ravenswaaij-Arts
D Majoor-Krakauer
M Angrist
A Chakravarti
C Meijers
C H Buys
(P2860) (Q24324643)
(Q24311512)
(Q28243225)
(Q24317184)
(Q34336251)
(Q34328245)
(Q57268200)
(Q24339000)
(Q50522919)
(Q72795387)
(Q28279279)
(Q72128453)
(Q57200656)
(Q57199537)
(Q28586637)
other details
description scientific article

External Links