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A. A. Redha

Observed names: A Redha, Abdulla Redha, Abdullah M. Redha
OpenAlex ID: A5017374662
Analysis of the origin of Turner's syndrome using polymorphic DNA probes.
1991 · S A Loughlin, A Redha, et al. · Journal of Medical Genetics · 48
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Alagille syndrome with de Novo del(20) (p 11.2)
1992 · Ahmad S. Teebi, D. S. Krishna Murthy, et al. · American Journal of Medical Genetics · 24
Disease profile of 400 institutionalized mentally retarded patients in Kuwait
1993 · T. I. Farag, S. A. Al‐Awadi, et al. · Clinical Genetics · 18
Primary ciliary dyskinesia: Kartagener syndrome in a family with a novel DNAH5 gene mutation and variable phenotypes
2014 · Makia J. Marafie, Ibrahim S. Al Suliman, et al. · Egyptian Journal of Medical Human Genetics · 7
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A germline RET proto-oncogene mutation in multiple members of an Arab family with variable onset of MEN type 2A-associated clinical manifestations
2016 · Makia Marafie, Ibrahim Suliman, et al. · Egyptian Journal of Medical Human Genetics
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Partial trisomy of short arm of chromosome 8 (46,XY, inv dup (8) (p21→pter) in a Bedouin child with multiple congenital anomalies and mental retardation
1994 · A. A. Redha, D. S. Krishna Murthy, et al. · The Indian Journal of Pediatrics
Works count: 6
Citation count: 97
H-index: 4
I10-index: 3
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