Format
Sort by

Send to

Choose Destination

Links from Books

Items: 2

1.

Deletion 3q22.1-q23 with blepharophimosis, ptosis and epicanthus inversus and an Albright hereditary osteodystrophy-like brachydactyly phenotype.

Croft MS, Turnpenny PD.

Clin Dysmorphol. 2008 Jul;17(3):189-91. doi: 10.1097/MCD.0b013e3282f4a984. No abstract available.

PMID:
18541966
2.

Familial insertional translocation of a portion of 3q into 11q resulting in duplication and deletion of region 3q22.1 leads to q24 in different offspring.

Williamson RA, Donlan MA, Dolan CR, Thuline HC, Harrison MT, Hall JG.

Am J Med Genet. 1981;9(2):105-11.

PMID:
7258223

Supplemental Content

Support Center