De novo duplication 1q32-q42: variability of phenotypic features in partial lq trisomics.

Author:

Lungarotti M S,Falorni A,Calabro A,Passalacqua F,Dallapiccola B

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference37 articles.

1. somique: Ins(7; 3) (q31; p21p26),1972

2. Clinical syndromes associated with partial duplications of chromosomes 2 and 3; dup(2p);Francke, U.,1978

3. Trisomy for the distal end of the short arm of chromosome 3. A syndrome;Yunis, J.J.;Am J Dis Child; 132: A number of structural variations and anomalies of chromosome 1 have been reported.' Among duplications of the long arm (lq +), the I qh variant is the most common.2 3The enlargement of chromosome 1 is in these instances the result of an elongation of the 30-3,1978

4. A familial 3/18 reciprocal translocation resulting in chromosome duplication-deficiency (3 ? + 18q-);Aarskog, D.;Acta Paediatr Scand

5. Among congenital anomalies of the long arm of cytes cultures from human peripheral blood;Exp Cell Res,1960

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