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2007 | 1 |
2008 | 1 |
2011 | 1 |
2024 | 0 |
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Page 1
Measurement of the clinical utility of a combined mutation detection protocol in carriers of Duchenne and Becker muscular dystrophy.
J Med Genet. 2007 Jun;44(6):368-72. doi: 10.1136/jmg.2006.047464. Epub 2007 Jan 26.
J Med Genet. 2007.
PMID: 17259292
Free PMC article.
A comparison of molecular and cytogenetic techniques for the diagnosis of pregnancy loss.
Caramins MC, Saville T, Shakeshaft R, Mullan GL, Miller B, Yip MY, Buckley MF.
Caramins MC, et al. Among authors: mullan gl.
Genet Med. 2011 Jan;13(1):46-51. doi: 10.1097/GIM.0b013e3181faa0d2.
Genet Med. 2011.
PMID: 21102343
Free article.
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Pfeiffer syndrome with neonatal death secondary to tracheal obstruction owing to the FGFR2 Glu565Ala mutation.
Freeman L, Elakis G, Watson G, Mullan GL, Taylor PJ, Anderson P, Ogle R, Buckley MF, Roscioli T.
Freeman L, et al. Among authors: mullan gl.
Clin Dysmorphol. 2008 Jul;17(3):223-224. doi: 10.1097/MCD.0b013e3282fdcc86.
Clin Dysmorphol. 2008.
PMID: 18541976
No abstract available.
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