1. Achieving orphan designation for placental insufficiency: annual incidence estimations in Europe. (6th February 2019) Authors: Spencer, R; Rossi, C; Lees, M; Peebles, D; Brocklehurst, P; Martin, J; Hansson, SR; Hecher, K; Marsal, K; Figueras, F; Gratacos, E; David, AL Journal: BJOG Issue: Volume 126:Number 9(2019) Page Start: 1157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Colour Atlas of Genetics: 2nd edition. Eberhard Passarge. (Pp 457.) Stuttgart: Thieme. 2001. ISBN 3-13-100362-6. New York: Thieme. 2001. ISBN 0-86577-958-9. Issue 1 (1st January 2002) Authors: Lees, M Journal: Journal of medical genetics Issue: Volume 39:Issue 1(2002) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Optic disc anomalies and frontonasal dysplasia. Issue 3 (1st March 1998) Authors: Hodgkins, P; Lees, M; Lawson, J; Reardon, W; Leitch, J; Thorogood, P; Winter, R M; Taylor, D S I Journal: British journal of ophthalmology Issue: Volume 82:Issue 3(1998) Page Start: 290 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locus. (19th April 2013) Authors: Holman, SK; Morgan, T; Baujat, G; Cormier‐Daire, V; Cho, T‐J; Lees, M; Samanich, J; Tapon, D; Hove, HD; Hing, A; Hennekam, R; Robertson, SP Journal: Clinical genetics Issue: Volume 83:Number 3(2013:Mar.) Page Start: 251 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locus. (5th July 2012) Authors: Holman, SK; Morgan, T; Baujat, G; Cormier‐Daire, V; Cho, T‐J; Lees, M; Samanich, J; Tapon, D; Hove, HD; Hing, A; Hennekam, R; Robertson, SP Journal: Clinical genetics Issue: Volume 83:Number 3(2013:Mar.) Page Start: 251 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Sponastrime dysplasia: presentation in infancy. Issue 12 (1st December 2001) Authors: Offiah, A C; Lees, M; Winter, R M; Hall, C M Journal: Journal of medical genetics Issue: Volume 38:Issue 12(2001) Page Start: 889 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene. Issue 5 (9th September 2005) Authors: Hoornaert, K P; Dewinter, C; Vereecke, I; Beemer, F A; Courtens, W; Fryer, A; Fryssira, H; Lees, M; Müllner-Eidenböck, A; Rimoin, D L; Siderius, L; Superti-Furga, A; Temple, K; Willems, P J; Zankl, A; Zweier, C; De Paepe, A; Coucke, P; Mortier, G R Journal: Journal of medical genetics Issue: Volume 43:Issue 5(2006) Page Start: 406 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. X‐linked CHARGE‐like Abruzzo–Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations. (19th April 2013) Authors: Pauws, E; Peskett, E; Boissin, C; Hoshino, A; Mengrelis, K; Carta, E; Abruzzo, MA; Lees, M; Moore, GE; Erickson, RP; Stanier, P Journal: Clinical genetics Issue: Volume 83:Number 4(2013:Apr.) Page Start: 352 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. X‐linked CHARGE‐like Abruzzo–Erickson syndrome and classic cleft palate with ankyloglossia result from TBX22 splicing mutations. (7th August 2012) Authors: Pauws, E; Peskett, E; Boissin, C; Hoshino, A; Mengrelis, K; Carta, E; Abruzzo, MA; Lees, M; Moore, GE; Erickson, RP; Stanier, P Journal: Clinical genetics Issue: Volume 83:Number 4(2013:Apr.) Page Start: 352 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗