Deletion 14q (q22q23) associated with anophthalmia, absent pituitary, and other abnormalities.

Author:

Bennett C P,Betts D R,Seller M J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference7 articles.

1. We thank Miss Raju, Consultant Obstetrician, for referring this patient, Dr N Fagg for the histology, and the Spastics Society for financial support

2. Two patients with interstitial del(l4q), one with features of Holt-Oram syndrome. Exclusion mapping of PI (alpha-l-antitrypsin);Turleau, C.; de Grouchy, J.; Chavin-Colin, F.;Ann Genet (Paris),1984

3. A case of partial monosomy 14q;Kawamura, G.; Suzuki, M.; Segawa, T.;J Pediatr Pract,1985

4. Deletion 14q(q24.3 to q32. 1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of Pi (a,-antitrypsin);Yamamoto, Y.; Sawa, R.; Okamoto, N.;Hun Genet,1986

5. A complex translocation involving chromosomes 3, 11 and 14 with an interstitial deletion, del(l4Xql3q22) in a child with congenital glaucoma and cleft lip and palate;Buchanan, P.D.; Rao, K.W.; Doerr, C.L.; etal,1978

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