Author:
Bijlsma Jan B.,de France Henny F.,Bleeker-Wagemakers Liesbeth M.,Dijkstra Piet F.
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference22 articles.
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2. Allderdice, P. W., Miller, O. J., Miller, D. A.: Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence. Humangenetik 13, 205?209 (1971)
3. Armendares, S., Salamanca, F., Nava, S., Ramirez, S., Cantu, J.-M.: Le syndrome de la trisomie 12p. Ann. Génét. 18, 89?94 (1975)
4. Bell, E. F., Warburton, D.: Two reciprocal translocations associated with microcephaly and retardation. J. Med. Genet. 14, 141?142 (1977)
5. Biederman, B., Bowen, P., Robertson, C., Schiff, D.: Partial trisomy 12p due to t(12;21)pat translocation. Hum. Genet. 36, 35?41 (1977)
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