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Group by: Author | Type
Jump to: K | L | M | P
Number of items: 7.

K

Kelberman, D.; Rizzoti, K.; Avilion, A.; Bitner-Glindzicz, M.; Cianfarani, S.; Collins, J.; Chong, W.K.; (2006) Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans. Journal of Clinical Investigation , 116 (9) pp. 2422-2455. 10.1172/JCI28658. Green open access
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L

Lim, J.C.S.T.; (2006) The genetic basis of hemifacial microsomia. Doctoral thesis, University of London. Green open access
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M

Mills, K.; Mills, P.; Jackson, M.; Worthington, V.; Beesley, C.; Mann, A.; Clayton, P.; (2006) Diagnosis of congenital disorders of glycosylation type-I using protein chip technology. Proteomics , 6 (7) pp. 2295-2304. 10.1002/pmic.200500682.

Mills, K.; Mills, P.; Jackson, M.; Worthington, V.; Beesley, C.; Mann, A.; Clayton, P.; (2006) Diagnosis of congenital disorders of glycosylation type-I using protein chip technology. PROTEOMICS , 6 (7) pp. 2295-2304. 10.1002/pmic.200500682.

Monk, D.; Arnaud, P.; Apostolidou, S.; Hills, F.A.; Kelsey, G.; Stanier, P.; Feil, R.; (2006) From the Cover: limited evolutionary conservation of imprinting in the human placenta. Proceedings of the National Academy of Sciences , 103 (17) pp. 6623-6628. 10.1073/pnas.0511031103.

P

PEREZ-MIRANDA, A; García-Obregón, S; Alfonso-Sánchez, MA; Vidales, C; Arroyo, D; Peña, JA; (2006) Genetic position of Valencia (Spain) in the Mediterranean basin according to Alu insertions. American Journal of Human Biology , 18 (2) 187 - 195. 10.1002/ajhb.20487.

Pagnamenta, A.T.; Taanman, J.-W.; Wilson, C.J.; Anderson, N.E.; Marotta, R.; Duncan, A.J.; Bitner- Glindzicz, M.; (2006) Dominant inheritance of premature ovarian failure associated with mutant mitochondrial DNA polymerase gamma. Human Reproduction , 21 (10) pp. 2467-2473. 10.1093/humrep/del076.

This list was generated on Sun Apr 24 05:48:50 2016 BST.