Clinical features and mental development of a child with a prenatally identified 45,XX,der(5)t(5;18) (p15;q11.2),-18 karyotype.

Author:

Hutcheon R G,Mallik A,Shaham M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference7 articles.

1. The cri-du-chat syndrome: epidemiology, cytogenetics, and clinical features;Niebuhr, E.;Hum Genet,1978

2. Psychomotor development in 65 home-reared children with cri-du-chat syndrome;Wilkins, L.E.; Brown, J.A.; Wolf, B.;Pediatr,1980

3. Molecular definition of deletions of different segments of distal 5p that result in distinct phenotype features;Church, D.M.; Bengtsson, U.; Nielsen, K.V.; Wasmuth, J.J.; Niebuhr, E.;Am Hum Genet,1995

4. Evidence for a distinct region causing a catlike cry in patients with 5p deletions;Gersh, M.; Goodart, S.A.; Pasztor, L.M.; Harris, D.J.; Weiss, L.; Overhauser, J.;Am Jf Hum Genet,1995

5. Chromosome 18, monosomy 18p;Greenberg, F.,1990

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