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Is Part Of Case reports in genetics. Volume 2012(2012)

3. Autism Spectrum Disorder in a Girl with a De Novo X;19 Balanced Translocation. (17th May 2012)

Authors:
Baruffi, Marcelo Razera; de Souza, Deise Helena; Bicudo da Silva, Rosana Aparecida; Ramos, Ester Silveira; Moretti-Ferreira, Danilo
Other Names:
Baumer A. Academic Editor.; Bunyan D. J. Academic Editor.; López Ginés C. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2012(2012)
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Journal Article
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5. Detection of Chromosome X;18 Breakpoints and Translocation of the Xq22.3;18q23 Regions Resulting in Variable Fertility Phenotypes. (8th February 2012)

Authors:
Szvetko, Attila; Martin, Nicole; Joy, Chris; Hayward, Andrea; Watson, Bob; Cary, Andrew; Withers, Stephen
Other Names:
Bunyan D. J. Academic Editor.; López Ginés C. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2012(2012)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Early Intervention Combined with Targeted Treatment Promotes Cognitive and Behavioral Improvements in Young Children with Fragile X Syndrome. (26th March 2012)

Authors:
Winarni, Tri Indah; Schneider, Andrea; Borodyanskara, Mariya; Hagerman, Randi J.
Other Names:
Kubota T. Academic Editor.; Shotelersuk V. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2012(2012)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

7. Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome. (25th March 2012)

Authors:
Hernandes, Marina Araújo Fonzar; Marques-Salles, Terezinha de Jesus; Mkrtchyan, Hasmik; Soares-Ventura, Eliane Maria; Leite, Edinalva Pereira; Muniz, Maria Tereza Cartaxo; Cornélio, Maria Teresa Marquim Nogueira; Liehr, Thomas; Santos, Neide; Silva, Maria Luiza Macedo
Other Names:
López Ginés C. Academic Editor.; Saccucci P. Academic Editor.; Velagaleti G. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2012(2012)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

8. Gain of Chromosome 4qter and Loss of 5pter: An Unusual Case with Features of Cri du Chat Syndrome. (20th December 2012)

Authors:
Sheth, Frenny; Gohel, Naresh; Liehr, Thomas; Akinde, Olakanmi; Desai, Manisha; Adeteye, Olawaleye; Sheth, Jayesh
Other Names:
Bunyan D. J. Academic Editor.; Ergul E. Academic Editor.; Fenger M. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2012(2012)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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