Recurrence risks in mental retardation.

di Crow, Y J, Tolmie, J L
Pubblicazione 1998

Insulin dependent diabetes in childhood and material deprivation in northern England, 1977-86.

di Crow, Y J, Alberti, K G, Parkin, J M
Pubblicazione 1991

Therapies in Aicardi–Goutières syndrome

di Crow, Y J, Vanderver, A, Orcesi, S, Kuijpers, T W, Rice, G I
Pubblicazione 2014

Aicardi-Goutières Syndrome: Neuroradiologic Findings and Follow-Up

di Uggetti, C., La Piana, R., Orcesi, S., Egitto, M.G., Crow, Y.J., Fazzi, E.
Pubblicato in AJNR Am J Neuroradiol (2009)

A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.

di Ghaffari, S R, Boyd, E, Tolmie, J L, Crow, Y J, Trainer, A H, Connor, J M
Pubblicazione 1998

Treatment of Gastrointestinal Bleeding in a Probable Case of Cerebroretinal Microangiopathy with Calcifications and Cysts

di Briggs, T.A., Hubbard, M., Hawkins, C., Cole, T., Livingston, J.H., Crow, Y.J., Pigott, A.
Pubblicazione 2011

"Cataplexy" and muscle ultrasound abnormalities in Coffin-Lowry syndrome.

di Crow, Y J, Zuberi, S M, McWilliam, R, Tolmie, J L, Hollman, A, Pohl, K, Stephenson, J B
Pubblicazione 1998

Type 1 interferonopathy presenting as juvenile idiopathic arthritis with interstitial lung disease: report of a new phenotype

di Clarke, S. L. N., Robertson, L., Rice, G. I., Seabra, L., Hilliard, T. N., Crow, Y. J., Ramanan, A. V.
Pubblicato in Pediatr Rheumatol Online J (2020)

Sharing of PPT mutations between distinct clinical forms of neuronal ceroid lipofuscinoses in patients from Scotland.

di Munroe, P B, Greene, N D, Leung, K Y, Mole, S E, Gardiner, R M, Mitchison, H M, Stephenson, J B, Crow, Y J
Pubblicazione 1998

ADA2 deficiency: case report of a new phenotype and novel mutation in two sisters

di Uettwiller, F, Sarrabay, G, Rodero, M P, Rice, G I, Lagrue, E, Marot, Y, Deiva, K, Touitou, I, Crow, Y J, Quartier, P
Pubblicato in RMD Open (2016)

Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi–Goutières and Singleton–Merten syndromes

di Bursztejn, A.-C., Briggs, T.A., del Toro Duany, Y., Anderson, B.H., O’Sullivan, J., Williams, S.G., Bodemer, C., Fraitag, S., Gebhard, F., Leheup, B., Lemelle, I., Oojageer, A., Raffo, E., Schmitt, E., Rice, G.I., Hur, S., Crow, Y.J.
Pubblicato in Br J Dermatol (2015)

A second locus for Aicardi‐Goutières syndrome at chromosome 13q14–21

di Ali, M, Highet, L J, Lacombe, D, Goizet, C, King, M D, Tacke, U, van der Knaap, M S, Lagae, L, Rittey, C, Brunner, H G, van Bokhoven, H, Hamel, B, Oade, Y A, Sanchis, A, Desguerre, I, Cau, D, Mathieu, N, Moutard, M L, Lebon, P, Kumar, D, Jackson, A P, Crow, Y J
Pubblicazione 2006

Aicardi-Goutières Syndrome Displays Genetic Heterogeneity with One Locus (AGS1) on Chromosome 3p21

di Crow, Y. J., Jackson, A. P., Roberts, E., van Beusekom, E., Barth, P., Corry, P., Ferrie, C. D., Hamel, B. C. J., Jayatunga, R., Karbani, G., Kálmánchey, R., Kelemen, A., King, M., Kumar, R., Livingstone, J., Massey, R., McWilliam, R., Meager, A., Rittey, C., Stephenson, J. B. P., Tolmie, J. L., Verrips, A., Voit, T., van Bokhoven, H., Brunner, H. G., Woods, C. G.
Pubblicazione 2000