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Tel Hashomer camptodactyly syndrome in identical twin infants.
Smolkin T, Blazer S, Gershoni-Baruch R, Makhoul IR. Smolkin T, et al. Among authors: blazer s. Clin Dysmorphol. 2011 Oct;20(4):214-216. doi: 10.1097/MCD.0b013e32834a044f. Clin Dysmorphol. 2011. PMID: 21814136 Review. No abstract available.
Rare presentations of congenital hypothyroidism.
Smolkin T, Ulanovsky I, Blazer S, Makhoul IR. Smolkin T, et al. Among authors: blazer s. Isr Med Assoc J. 2011 Dec;13(12):779-80. Isr Med Assoc J. 2011. PMID: 22332453 Free article. No abstract available.
'Pure' partial trisomy 11q (11q23.1→11qter): expanding the phenotype.
Zimberg-Bossira A, Smolkin T, Gildish A, Moustafa-Hawash N, Blazer S, Gershoni-Baruch R, Makhoul IR. Zimberg-Bossira A, et al. Among authors: blazer s. Clin Dysmorphol. 2011 Oct;20(4):225-228. doi: 10.1097/MCD.0b013e328349bcf8. Clin Dysmorphol. 2011. PMID: 21900761 No abstract available.
106 results