Journal article

X-linked alpha thalassaemia/mental retardation syndrome: a case with gonadal dysgenesis, caused by a novel mutation in ATRX gene.

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APA Style

Jezela-Stanek, A., Fisher, C., Szarras-Czapnik, M., Olczak-Kowalczyk, D., Gibbons, R., Słowikowska-Hilczer, J., & Krajewska-Walasek, M. (2009). X-linked alpha thalassaemia/mental retardation syndrome: a case with gonadal dysgenesis, caused by a novel mutation in ATRX gene. Clinical Dysmorphology, 18(3), 168–171.

MLA Style

Jezela-Stanek, A, et al. “X-Linked Alpha Thalassaemia/Mental Retardation Syndrome: a Case with Gonadal Dysgenesis, Caused by a Novel Mutation in ATRX Gene.” Clinical Dysmorphology, vol. 18, no. 3, 2009, pp. 168–71.

Chicago Style

Jezela-Stanek, A, C Fisher, M Szarras-Czapnik, et al. 2009. “X-Linked Alpha Thalassaemia/Mental Retardation Syndrome: a Case with Gonadal Dysgenesis, Caused by a Novel Mutation in ATRX Gene.” Clinical Dysmorphology 18 (3): 168–71.
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Publisher copy:: 10.1097/mcd.0b013e32832a9ea5

Authors

+ Jezela-Stanek, A More by this author

Role:: Author

+ Fisher, C More by this author

Role:: Author

+ Szarras-Czapnik, M More by this author

Role:: Author

+ Olczak-Kowalczyk, D More by this author

Role:: Author

+ Gibbons, R More by this author

Role:: Author

More authors...

Journal:: Clinical dysmorphology More from this journal
Volume:: 18
Issue:: 3
Pages:: 168-171
Publication date:: 2009-07-01
DOI:: 10.1097/mcd.0b013e32832a9ea5
EISSN:: 1473-5717
ISSN:: 0962-8827

Language:: English
Keywords:: Genetic Diseases, X-Linked

Infant, Newborn

Intellectual Disability

Nuclear Proteins

Humans

alpha-Thalassemia

DNA Helicases

Mutation

Male

Gonadal Dysgenesis
Pubs id:: pubs:253726
UUID:: uuid:0c76438b-ea22-45c7-8f20-ac8bad3fb8dd
Local pid:: pubs:253726
Source identifiers:: 253726
Deposit date:: 2012-12-19
ARK identifier:: ark:/29072/ora_0c76438bea2245c78f20ac8bad3fb8dd

Terms of use

Copyright date:: 2009

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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