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Items: 3

1.

24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism.

Chen CP, Wang TH, Lin SP, Chern SR, Chen MR, Lee CC, Chen YJ, Wang W.

Eur J Med Genet. 2006 Nov-Dec;49(6):516-9. Epub 2006 May 15.

PMID:
16769261
2.

Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child.

Lorda-Sanchez I, Lopez-Pajares I, Roche MC, Sanz R, Rodriguez de Alba M, Gonzalez-Gonzalez MC, IbaƱez A, Ramos C, Ayuso C.

Am J Med Genet. 2000 Dec 11;95(4):336-8.

PMID:
11186887
3.

Dysmorphic sibs trisomic for the region 6q22.1-->6q23.3.

Goh DL, Tan AS, Chen JY, Van Den Berghe JA.

J Med Genet. 2000 Nov;37(11):889-92. No abstract available.

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