Commentary on Spriggs: genetically selected baby free of inherited predisposition to early onset Alzheimer's disease

Por Delatycki, M
Publicado em 2003

Response to Spriggs: Is conceiving a child to benefit another against the interest of the new child?

Por Delatycki, M
Publicado em 2005

Sperm donor suffers years later from inherited disease

Por Gebhardt, D, Delatycki, M.
Publicado em 2002

Friedreich ataxia: an overview

Por Delatycki, M., Williamson, R., Forrest, S.
Publicado em 2000

In response to Cadet et al

Por Delatycki, M B, Allen, K J
Publicado em 2006

When is it best to test? Attitudes of health professionals regarding genetic testing for Familial Adenomatous Polyposis (FAP)

Por Lynch E, Duncan RE, Macrae F, Delatycki M
Publicado em 2012-04-01

Sleep disturbance in Sanfilippo syndrome: a parental questionnaire study

Por Fraser, J, Gason, A, Wraith, J, Delatycki, M
Publicado em 2005

When is it best to test? Attitudes of health professionals regarding genetic testing for Familial Adenomatous Polyposis (FAP)

Por Lynch, E, Duncan, RE, Macrae, F, Delatycki, M
Publicado em 2012

De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bones

Por Delatycki, M, Danks, A, Churchyard, A, Zhou, X, Eng, C
Publicado em 2003

Ethical considerations in presymptomatic testing for variant CJD

Por Duncan, R, Delatycki, M, Collins, S, Boyd, A, Masters, C, Savulescu, J
Publicado em 2005

46,XX/46,XY at amniocentesis in a fetus with true hermaphroditism

Por AMOR, D., DELATYCKI, M., SUSMAN, M., CASEY, E., NASH, T., WARNE, G., HUTSON, J.
Publicado em 1999

How is disease progress in Friedreich's ataxia best measured? A study of four rating scales

Por Fahey, M C, Corben, L, Collins, V, Churchyard, A J, Delatycki, M B
Publicado em 2007

‘No thanks’—reasons why pregnant women declined an offer of cystic fibrosis carrier screening

Por Ioannou, L., Massie, J., Lewis, S., McClaren, B., Collins, V., Delatycki, M. B.
Publicado em 2013

Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection

Por Delatycki, M., Voullaire, L., Francis, D., Petrovic, V., Robertson, A., Webber, L., Slater, H.
Publicado em 1999

A novel pericentric inversion of chromosome 3 cosegregates with a developmental-behavioural phenotype

Por Efron, D, Delatycki, M, de Silva, M G, Langbein, A, Slaghuis, W, Larson, A, Dahl, H, Forrest, S
Publicado em 2003

Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA gene.

Por Delatycki, M B, Paris, D, Gardner, R J, Forshaw, K, Nicholson, G A, Nassif, N, Williamson, R, Forrest, S M
Publicado em 1998

Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene

Por Fahey, M, Knight, M, Shaw, J, Gardner, R, du Sart, D, Lockhart, P, Delatycki, M, Gates, P, Storey, E
Publicado em 2005

Disruption of a novel member of a sodium/hydrogen exchanger family and DOCK3 is associated with an attention deficit hyperactivity disorder-like phenotype

Por de Silva, M G, Elliott, K, Dahl, H, Fitzpatrick, E, Wilcox, S, Delatycki, M, Williamson, R, Efron, D, Lynch, M, Forrest, S
Publicado em 2003

A maternally transmitted lethal neonatal progeroid syndrome with prominent genitourinary and gastrointestinal features.

Por Delatycki, M B, Cleary, M A, Bankier, A, McDougall, P N, Ahluwalia, J S, Chow, C W, Cooke-Yarborough, C M
Publicado em 1997

Audit of routine immunohistochemistry testing for mismatch repair proteins at diagnosis of colorectal cancer under the age of 50

Por Lipton, L, Kentwell, M, Li, M, Williams, D, Christie, M, Landgren, A, Dow, C, Jones, I, McLaughlin, S, Delatycki, M, Macrae, F, Lynch, E
Publicado em 2012