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1.
Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2.
Eur J Hum Genet
; 11(11): 892-5, 2003 Nov.
Article
in English
| MEDLINE | ID: mdl-14571277
2.
A novel external fixator used to treat open comminuted fractures of the middle and distal phalanges with concomitant FDP avulsion injury.
Tech Hand Up Extrem Surg
; 18(3): 121-4, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24759632
3.
Does the proposed removal of mitotic count as a prognostic indicator in melanoma, accurately reflect the risk profile for metastasis in UK patients?
J Plast Reconstr Aesthet Surg
; 71(2): 261-262, 2018 02.
Article
in English
| MEDLINE | ID: mdl-29198981
4.
Further evidence supporting the need for improved risk stratification of thin melanoma.
J Plast Reconstr Aesthet Surg
; 70(7): 967-968, 2017 07.
Article
in English
| MEDLINE | ID: mdl-28455186
5.
Clinical dividends from the molecular genetic diagnosis of craniosynostosis.
Am J Med Genet A
; 143A(16): 1941-9, 2007 Aug 15.
Article
in English
| MEDLINE | ID: mdl-17621648
6.
Clinical dividends from the molecular genetic diagnosis of craniosynostosis.
Am J Med Genet A
; 140(23): 2631-9, 2006 Dec 01.
Article
in English
| MEDLINE | ID: mdl-16838304
7.
Paternal origin of FGFR3 mutations in Muenke-type craniosynostosis.
Hum Genet
; 115(3): 200-7, 2004 Aug.
Article
in English
| MEDLINE | ID: mdl-15241680
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