Identification of a submicroscopic 3.2 Mb chromosomal 16q12.2-13 deletion in a child with short stature, mild developmental delay, and craniofacial anomalies, by high-density oligonucleotide array-a recognizable syndrome
2010 ◽
Vol 152A
(9)
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pp. 2365-2371
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2001 ◽
Vol 7
(9)
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pp. 486-494
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1998 ◽
Vol 26
(21)
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pp. 4975-4982
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2002 ◽
Vol 129
(1)
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pp. 57-66
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Keyword(s):
2001 ◽
Vol 85
(1)
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pp. 107-114
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2006 ◽
Vol 101
(1)
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pp. 52-57
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Keyword(s):
2004 ◽
Vol 59
(4)
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pp. B306-B315
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