Molecular characterization and clinical features of a patient with an interstitial deletion of 3p25.3-p26.1

2010 ◽  
Vol 152A (12) ◽  
pp. 3110-3114 ◽  
Author(s):  
Cecilia Gunnarsson ◽  
Cathrine Foyn Bruun
Keyword(s):  
Molecular Characterization ◽  
Clinical Features ◽  
Interstitial Deletion

Molecular characterization of an 11q interstitial deletion in a patient with the clinical features of Jacobsen syndrome

2006 ◽  
Vol 140A (7) ◽  
pp. 704-708 ◽  
Author(s):  
Sharon L. Wenger ◽  
Paul D. Grossfeld ◽  
Benjamin L. Siu ◽  
James E. Coad ◽  
Frank G. Keller ◽  
...  
Keyword(s):  
Molecular Characterization ◽  
Clinical Features ◽  
Interstitial Deletion ◽  
Jacobsen Syndrome

Molecular characterization and clinical features of Chinese pulmonary sarcomatoid carcinoma: analysis of 36 cases.

2018 ◽  
Vol 36 (15_suppl) ◽  
pp. e13616-e13616
Author(s):  
Di Wu ◽  
Yingying Yu ◽  
Jiwei Liu ◽  
Wei Liu ◽  
Shijie Lan ◽  
...  
Keyword(s):  
Molecular Characterization ◽  
Clinical Features ◽  
Sarcomatoid Carcinoma ◽  
Pulmonary Sarcomatoid Carcinoma

Two cases of 11p13 interstitial deletion and unusual clinical features

2008 ◽  
Vol 26 (3) ◽  
pp. 247-249 ◽  
Author(s):  
K.-H. Gustavson ◽  
G. Annerén ◽  
L. Wranne
Keyword(s):  
Clinical Features ◽  
Interstitial Deletion

Interstitial deletion of 10q: Clinical features and literature review

1992 ◽  
Vol 43 (4) ◽  
pp. 701-703 ◽  
Author(s):  
Sandra Lobo ◽  
Jaroslav Cervenka ◽  
Arnold London ◽  
Mary Ella M. Pierpont
Keyword(s):  
Literature Review ◽  
Clinical Features ◽  
Interstitial Deletion

Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical features

2016 ◽  
Vol 59 (1) ◽  
pp. 39-42 ◽  
Author(s):  
Rosamaria Silipigni ◽  
Elisa Cattaneo ◽  
Marco Baccarin ◽  
Monica Fumagalli ◽  
Maria Francesca Bedeschi
Keyword(s):  
Developmental Delay ◽  
Clinical Features ◽  
Interstitial Deletion

Genetic Alterations in Childhood Melanoma

2012 ◽  
pp. 589-592
Author(s):  
Fariba Navid
Keyword(s):  
Molecular Characterization ◽  
Clinical Features ◽  
Population Based ◽  
Genetic Alterations ◽  
Single Institution ◽  
Therapeutic Value

Overview: Melanoma is rare in children. However, the clinical features of the disease in this population have been well-documented through single-institution experiences and population-based analyses. Still, our understanding of the etiologic factors in children remains unclear and diagnosis of melanoma remains challenging in certain cases. This article reviews emerging evidence indicating that molecular characterization of these lesions in children may be of diagnostic and therapeutic value.

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