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Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemia. [electronic resource] by
- Wat, Margaret J
- Enciso, Victoria B
- Wiszniewski, Wojciech
- Resnick, Trevor
- Bader, Patricia
- Roeder, Elizabeth R
- Freedenberg, Debra
- Brown, Chester
- Stankiewicz, Pawel
- Cheung, Sau-Wai
- Scott, Daryl A
Producer: 20110302
In:
Journal of medical genetics vol. 47
Availability: No items available.
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American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. [electronic resource] by
- Alford, Raye L
- Arnos, Kathleen S
- Fox, Michelle
- Lin, Jerry W
- Palmer, Christina G
- Pandya, Arti
- Rehm, Heidi L
- Robin, Nathaniel H
- Scott, Daryl A
- Yoshinaga-Itano, Christine
Producer: 20141205
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 16
Availability: No items available.
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