Clinical manifestations of trisomy 4p syndrome

Author:

Patel Sanjivan V.,Dagnew Hirut,Parekh Aruna J.,Koenig Eli,Conte Robert A.,Macera Michael J.,Verma Ram S.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference73 articles.

1. Anderson O, Lundsteen C, Niebuhr E (1981) A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4. Cytogenet Cell Genet 30: 3–10

2. Andre MJ, Aurias A, Barranger P de, Gillot F, LeFranc G, Lejeune J (1976) Trisomie 4p de novo para isochromosome 4p. Ann Genet 19:127–131

3. Andrle M, Erlach A, Killian W, Rett A (1976) Two cases of trisomy 4p with translocation t(4p-; 7q+) in several members of one family. Hum Genet 33: 155–160

4. Baccichetti C, Tenconi R, Caufin D, Bortotto L (1982) Study on segregation of the inversion of chromosome 4(p15.2q11) in two unrelated families. Hum Genet 63:117–120

5. Bauknecht T, Betteken F, Vogel W (1976) Trisomy 4p due to a paternal t(4p-; 16p+) translocation. Hum Genet 31:227–230

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