Comparative clinical studies and X chromosome behaviour in a case of XXXX-XXXXX mosaicism.

Author:

Cooke P,Black J A,Curtis D J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Double autosomal trisomy (D trisomy plus mongolism);Becker, K.L.; Burke, E.C.; Albert, A.,1963

2. Inhibition of the motility of gill cilia of Dreissensia by plasma of cystic fibrosis patients and their parents;Besley, G.T.N.; Patrick, A.D.; Norman, A.P.;Journal of Medical Genetics,1969

3. The use of quinacrine fluorescence in the identification of B and E group chromosomes involved in structural abnormalities;Bobrow, M.; Pearson, P.L.;J'ournal of Medical Genetics,1971

4. Pathologie comparee des trisomies D et E;Bocquet, L.,1968

5. Abnormal siblings in patients with trisomy 13-15 and 17-18;Campbell, J.B.;Military Medicine,1969

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. A new case of tetrasomy X in a 8 years old girl;Acta Endocrinologica (Bucharest);2012

2. Detailed analysis of X chromosome inactivation in a 49,XXXXX pentasomy;Molecular Cytogenetics;2009-10-07

3. Pentasomy X: Report of patient and studies of X-inactivation;American Journal of Medical Genetics;1981

4. The penta-X syndrome.;Journal of Medical Genetics;1980-10-01

5. Renal hypodysplasia and unilateral ovarian agenesis in the Penta-X syndrome;American Journal of Medical Genetics;1980

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