Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.-Reference-Cited by-同舟云学术

Molecular characterisation of chromosome 4p deletions resulting in Wolf-Hirschhorn syndrome.

Published:1994-02-01 Issue:2 Volume:31 Page:103-107
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Estabrooks L L,Lamb A N,Aylsworth A S,Callanan N P,Rao K W

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference15 articles.

1. The Wolf-Hirschhorn (4p-) syndrome;Johnson, V.P.; Mulder, R.D.; Hosen, R.;Clin Genet,1976

2. Genetic and clinical studies in 13 patients with the Wolf-Hirschhorn syndrome [del(4p)]. Hum Genet;Wilson, M.G.; Towner, J.W.; Coffin, G.S.,1981

3. A taxonomic approach to GutsheelldaelJ(F4, p)TpahnezniotRyEp, e. BaAdme]r_PMI, edet Genet 1985; 21: 337-45. al. Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome;Preus, M.; AymeS, Kaplan; P.;Nature,1985

4. Preferential paternal origin of de novo structural rearrangements;Olson, S.B.; Magenis, R.E.,1988

5. Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome;Quarrell, O.W.J.; Snell, R.G.; Curtis, M.A.;Med Genet,1991

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