Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome (Q34308670)
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(P31) (Q13442814)
(P50) (Q21165202)
(P304) 165-172
(P407) (Q1860)
(P433) 2
(P478) 9
(P577) Wednesday, February 1, 1995
(P921) (Q618246)
(P1433) (Q976454)
(P1476) "Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome" (language: en)
(P2093) Slaney SF
Oldridge M
Poole MD
Ashworth GJ
Hockley AD
Hayward RD
David DJ
Pulleyn LJ
Rutland P
(P2860) (Q57278686)
(Q28249477)
(Q24310222)
(Q24315050)
(Q24314986)
(Q52215435)
(Q52444686)
(Q28255555)
(Q34324097)
(Q46371402)
(Q34322623)
(Q45345175)
(Q52216584)
(Q56386843)
(Q24306718)
(Q28263694)
(Q28294978)
(Q27641409)
(Q55670928)
(Q33192755)
(Q25938986)
(Q28300015)
(Q46186049)
(Q56422636)
(Q38140616)
(Q40888817)
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(Q28237425)
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(Q72017465)
(Q68300805)
(Q48191319)
(Q24324199)
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(Q37935123)
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(Q71642294)
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(Q28776010)
(Q33280838)
(Q30958672)
(Q48086215)
(Q48176091)
(Q35814879)
(Q40505519)
(Q53484458)
(Q58827851)
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