Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23 (Q24517956)
scientific article published on August 1, 1998
Language:
(P31) (Q13442814)
(P304) 617-23
(P407) (Q1860)
(P433) 8
(P478) 35
(P577) +1998-08-00T00:00:00Z
(P921) (Q431643)
(Q638893)
(P953) https://jmg.bmj.com/content/jmedgenet/35/8/617.full.pdf
https://europepmc.org/articles/PMC1051383
https://europepmc.org/articles/PMC1051383?pdf=render
https://syndication.highwire.org/content/doi/10.1136/jmg.35.8.617
(P1433) (Q14640281)
(P1476) "Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23" (language: en)
(P2093) D. R. Mowat
G. D. Croaker
D. T. Cass
B. A. Kerr
J. Chaitow
L. C. Adès
N. L. Chia
M. J. Wilson
(P2860) (Q24311237)
(Q24324643)
(Q24311512)
(Q28295097)
(Q28295089)
(Q28279279)
(Q28278792)
(Q27860812)
(Q34336251)
(Q34726074)
(Q40441414)
(Q34717965)
(Q39811525)
(Q33677026)
(Q37991720)
(Q36940673)
(Q52099999)
(Q52096961)
(Q45344091)
(Q67053163)
(Q71267581)
(Q69564416)
(Q68044310)
(Q57199537)
other details
description scientific article published on August 1, 1998

External Links