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Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

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Year: 1987
Type: article
Study design: Observational Study
Source: Human Genetics
DOI: 10.1007/bf00281063
Authors: Anthony P. Monaco, Corlee J. Bertelson, Chris Colletti-Feener, Louis M. Kunkel
Institutions: Boston Children's Hospital, Harvard University
Language: English

Topic: Muscle Physiology and Disorders
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Awards: G3446264458, Medical Scientist Training Program, G573904840, G689141124
OpenAlex ID: W1971535185
FWCI: 10.33
Cites: 34
Cited by: 133
Related to: 10
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