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Author/Creator Cheng C.-W. Academic Editor.

1. A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband. (12th September 2011)

Authors:
Wilson, Nicole K. A.; Lee, Yohan; Long, Robert; Hermetz, Karen; Rudd, M. Katharine; Miller, Rachel; Rapoport, Judith L.; Addington, Anjené M.
Other Names:
Cheng C.-W. Academic Editor.; Ergul E. Academic Editor.; Steinberger D. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2011(2011)
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Journal Article
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2. Bilateral Radial Ulnar Synostosis and Vertebral Anomalies in a Child with a De Novo 16p13.3 Interstitial Deletion. (1st July 2013)

Authors:
Tam, Allison; Lee, Kit Shan; Lee, Sansan; Burkhalter, William; Pascua, Lucio U.; Slavin, Thomas P.
Other Names:
Bunyan D. J. Academic Editor.; Cheng C.-W. Academic Editor.; Cotter P. D. Academic Editor.; DeWan A. Academic Editor.; Wang X. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2013(2013)
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Journal Article
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3. Idiopathic Central Precocious Puberty Associated with 11 Mb De Novo Distal Deletion of the Chromosome 9 Short Arm. (30th July 2013)

Authors:
Cisternino, Mariangela; Della Mina, Erika; Losa, Laura; Madè, Alexandra; Rossetti, Giulia; Bassi, Lorenzo Andrea; Pieri, Giovanni; Bayindir, Baran; Messa, Jole; Zuffardi, Orsetta; Ciccone, Roberto
Other Names:
Bunyan D. J. Academic Editor.; Cheng C.-W. Academic Editor.; Morrison P. Academic Editor.; Velinov M. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2013(2013)
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Journal Article
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4. Novel SMAD3 Mutation in a Patient with Hypoplastic Left Heart Syndrome with Significant Aortic Aneurysm. (3rd March 2014)

Authors:
Fitzgerald, Kristi K.; Bhat, Abdul Majeed; Conard, Katrina; Hyland, James; Pizarro, Christian
Other Names:
Cheng C.-W. Academic Editor.; Fenger M. Academic Editor.; Huang C.-S. Academic Editor.; Morrison P. Academic Editor.; Vogt G. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2014(2014)
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Journal Article
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5. Recombinant Chromosome 4 from a Familial Pericentric Inversion: Prenatal and Adulthood Wolf-Hirschhorn Phenotypes. (16th May 2013)

Authors:
Malvestiti, Francesca; Benedicenti, Francesco; De Toffol, Simona; Chinetti, Sara; Höller, Adelheid; Grimi, Beatrice; Fichtel, Gertrud; Braghetto, Monica; Agrati, Cristina; Bonaparte, Eleonora; Maggi, Federico; Simoni, Giuseppe; Grati, Francesca Romana
Other Names:
Chae S.-C. Academic Editor.; Cheng C.-W. Academic Editor.; Cotter P. D. Academic Editor.; Fenger M. Academic Editor.; Morrison P. Academic Editor.; Vogt G. Academic Editor.; Wang X. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2013(2013)
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Journal Article
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6. Trichorhinophalangeal Syndrome Type I: A Patient with Two Novel and Different Mutations in the TRPS1 Gene. (17th April 2013)

Authors:
Dias, Catarina; Isidoro, Lara; Santos, Mafalda; Santos, Helena; Marques, Jorge Sales
Other Names:
Bunyan D. J. Academic Editor.; Cheng C.-W. Academic Editor.; Cotter P. D. Academic Editor.; Grant S. F. Academic Editor.; Velagaleti G. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2013(2013)
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Journal Article
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7. Unique Case Reports Associated with Ovarian Failure: Necessity of Two Intact X Chromosomes. (11th April 2012)

Authors:
Rao Kandukuri, Lakshmi; Padmalatha, Venkata; Kanakavalli, Murthy; Turlapati, Raseswari; Swapna, Mangalipally; Vidyadhari, Metuku; Saranaya, Govindaraghavan; Himaja, Kattera; Deenadayal, Mamata; Kumar Sethi, Bipin; Deb, Prasun; Gupta, Nalini; Chakraborthy, Baidyanath; Nallari, Pratibha; Singh, Lalji
Other Names:
Baumer A. Academic Editor.; Cheng C.-W. Academic Editor.; Cotter P. D. Academic Editor.; Saccucci P. Academic Editor.; Sazci A. Academic Editor.; Vogt G. Academic Editor.
Journal:
Case reports in genetics
Issue:
Volume 2012(2012)
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Record Type:
Journal Article
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