Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.

Author:

Zatz M,Vianna-Morgante A M,Campos P,Diament A J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference65 articles.

1. Clinical manifestations in two carriers of Duchenne muscular dystrophy;Emery, A.E.H.;Lancet,1963

2. Manifestations of Duchenne muscular dystrophy in carriers. In: Progress in neuro-genetics;Murphy, E.G.; Thompson, M.W.,1967

3. Frota-Pessoa 0. Clinical symptoms in a female carrier of Duchenne muscular dystrophy;Zatz, M.; Levisky, R.B.; Levy, J.A.; Valente, B.O.; Gianotti, M.;J Genet Hum,1973

4. Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with Xlinked muscular dystrophies (Duchenne and Becker);Zatz, M.; Shapiro, L.J.; Campion, D.S.; Kaback, M.M.; Otto, P.A.;J Neurol Sci,1980

5. Duchenne muscular dystrophy: genetic aspects, carrier detection and antenatal diagnosis;Emery, A.E.H.;Br Med Bull,1980

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1. Whole-Genome Sequencing Identified New Structural Variations in the DMD Gene That Cause Duchenne Muscular Dystrophy in Two Girls;International Journal of Molecular Sciences;2023-09-01

2. An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient;International Journal of Molecular Sciences;2022-10-28

3. Clinicopathologic and molecular profiles of Duchenne and Becker muscular dystrophy;Paediatrica Indonesiana;2019-09-24

4. Skewed X-inactivation is common in the general female population;European Journal of Human Genetics;2018-12-14

5. Genetics;Principles and Applications of Molecular Diagnostics;2018

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