De novo ring chromosome 6 in a child with multiple congenital anomalies.

Autor: Ahzad HA; Human Genetics Unit, Advanced Medical and Dental Institute, Universiti Sains Malaysia, Lot 29, Taman Bertam Indah, Kepala Batas, Penang, Malaysia., Ramli SF, Loong TM, Salahshourifar I, Zilfalil BA, Yusoff NM

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Periventricular heterotopia and white matter abnormalities in a girl with mosaic ring chromosome 6.

Autor: Satsuki Nishigaki¹ nishigaki.satsuki@med.osaka-cu.ac.jp, Takashi Hamazaki¹, Mika Saito¹, Toshiyuki Yamamoto², Toshiyuki Seto¹, Haruo Shintaku¹

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Gray Matter Heterotopia, Mental Retardation, Developmental Delay, Microcephaly, and Facial Dysmorphisms in a Boy with Ring Chromosome 6: A 10-Year Follow-Up and Literature Review.

Autor: Liu, Shu, Wang, Zhiqing, Wei, Sisi, Liang, Jinqun, Chen, Nuan, OuYang, Haimei, Zeng, Weihong, Chen, Liying, Xie, Xunjie, Jiang, Jianhui

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Frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies syndrome with a partial 21q22.3 deletion.

Autor: Guion-Almeida, Maria Leine, Richieri-Costa, Antonio, Jehee, Fernanda Sarquis, Passos-Bueno, Maria Rita Santos, Zechi-Ceide, Roseli Maria

Publikováno v: American Journal of Medical Genetics. Part A; Jul2012, Vol. 158A Issue 7, p1676-1679, 4p