Holt-Oram Syndrome
Hamiyet Pekel, Hidayet Durmaz
- Year : 1989
- Vol : 5
- Issue : 2
- Page :
147-150
A maIe child who had a skeletal and cardiovascular anomaly relaled with Synrome and esotropia was presented. On !his palient following symptoms were observed; bilaterally hypoplasique arm, 3 fingers on the right and 4 flngers on the left hand, arrioseptal defect and on the. eye 35 prisin diopri esoıropia, in the pedigri, tl was stated that was a first mutation occurred in mother.
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None of the authors, any product mentioned in this article,
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Holt-Oram Syndrome
1989,
Vol.
5
(2)
Received : 23.11.1989,
Accepted : 23.11.1989,
Published Online : 23.11.2020
Selçuk Tıp Dergisi
ISSN:1017-6616;
E-ISSN:2149-8059;