Browsing publications by Dr Mark Clement-Jones

Newcastle AuthorsTitleYearFull text
Dr Helen Phillips
Glenn Renforth
Dr Matthew Jackson
Dr Mark Clement-Jones
Dr David Wilson
et al.
Characterisation of a novel gene on distal 11q as a potential candidate for Hypoplastic Left Heart Syndrome2001
Dr Elizabeth Jones
Dr Mark Clement-Jones
Emeritus Professor Oliver James
Dr David Wilson
Differences between human and mouse alpha-fetoprotein expression during early development2001
Dr Gavin Clowry
Gordon Arnott
Dr Mark Clement-Jones
Changing pattern of expression of parvalbumin immunoreactivity during human fetal spinal cord development2000
Dr Elizabeth Jones
Dr Mark Clement-Jones
Dr David Wilson
JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype2000
Dr Neil Hanley
Dr Donna Hagan
Dr Mark Clement-Jones
Dr Stephen Ball
Professor Tom Strachan
et al.
SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development2000
Dr Mark Clement-Jones
Professor Stephen Robson
Professor Tom Strachan
Professor Susan Lindsay
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome2000
Dr Elizabeth Jones
Dr Mark Clement-Jones
Professor Susan Lindsay
Professor Tom Strachan
Professor Stephen Robson
et al.
Embryonic alphafetoprotein expression: Significant human and mouse differences1999
Dr Neil Hanley
Dr Stephen Ball
Dr Mark Clement-Jones
Dr Donna Hagan
Professor Tom Strachan
et al.
Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination1999
Professor Susan Lindsay
Dr Mark Clement-Jones
Professor Stephen Robson
Professor Tom Strachan
Expression of the short stature homeobox gene, SHOX, correlates with skeletal abnormalities in Turner syndromece1999
Dr Neil Hanley
Karen Piper
Dr Stephen Ball
Dr Mark Clement-Jones
Professor Tom Strachan
et al.
High level SOX9 expression during development of the human embryonic pancreas is associated with abnormal islet formation in a case of Campomelic Dysplasia.1999
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