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Search Results - Burren, C.P
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Mild phenotype and spontaneous improvement in a new form of perinatal hypophosphatasia with a novel recessive mutation in the TNSAP gene
by
Scurr, I.J
,
Burren, C.P
,
Soothill, P
,
Overton, T
,
Denbow, M
,
Grier, D
,
Gargan, M.F
,
Mornet, E
,
Smithson, S.F
Published in
Bone (New York, N.Y.)
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Monitoring Skull Base Abnormalities in Children with Osteogenesis Imperfecta – Review of Current Practice and a Suggested Clinical Pathway
by
Wadanamby, S.
,
El Garwany, S.
,
Connolly, DJA
,
Arundel, P.
,
Bishop, N.J.
,
DeVile, CJ
,
Calder, A.D.
,
Crowe, B.
,
Burren, C.P.
,
Saraff, V.
,
Offiah, A.C.
Published in
Bone (New York, N.Y.)
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Backache in a Duchenne boy
by
Kinali, M
,
Robinson, R
,
Manzur, A.Y
,
Burren, C.P
,
Robb, S.A
Published in
Neuromuscular disorders : NMD
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High prevalence of Somali population in children presenting with vitamin D deficiency in the UK
by
Modgil, G
,
Williams, B
,
Oakley, G
,
Burren, C P
Published in
Archives of disease in childhood
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Oesophageal septum and intramural distal tracheo-oesophageal fistula
by
BURREN, C. P
,
BEASLEY, S. W
Published in
Pediatric surgery international
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Neural tube defects induced by folate deficiency in mutant curly tail (Grhl3) embryos are associated with alteration in folate one-carbon metabolism but are unlikely to result from...
by
De Castro, Sandra C. P.
,
Leung, Kit-yi
,
Savery, Dawn
,
Burren, Katie
,
Rozen, Rima
,
Copp, Andrew J.
,
Greene, Nicholas D. E.
Published in
Birth defects research. A Clinical and molecular teratology
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