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Trisomy 1q and hematologic disorders

✍ Scribed by F. Anglani; L. Artifoni; L. Zanesco; C. Baccichetti; R. Tenconi


Book ID
119102517
Publisher
Elsevier Science
Year
1981
Tongue
English
Weight
638 KB
Volume
4
Category
Article
ISSN
0165-4608

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A male infant with partial trisomy 1q syndrome (46,XY,der(21),t(1;21)(q25;q22)pat) is described. Clinical findings include small for gestational age, hypoglycemia, ocular hypertelorism, microphthalmia, coloboma of the iris, low-set ears, beak nose, micrognathia, micropenis, cryptorchidism, presacral