The Experts below are selected from a list of 1977 Experts worldwide ranked by ideXlab platform
G G Haddad - One of the best experts on this subject based on the ideXlab platform.
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unusual inheritance of primary ciliary Dyskinesia kartagener s Syndrome
Journal of Medical Genetics, 1994Co-Authors: Deepak Narayan, S N Krishnan, M Upender, T S Ravikumar, M J Mahoney, T F Dolan, A S Teebi, G G HaddadAbstract:Primary ciliary Dyskinesia Syndrome is characterised by chronic sinusitis, bronchiectasis, and, in 50% of cases, dextrocardia. It is generally believed to be inherited as an autosomal recessive disorder. In this report, we describe a family consisting of a mother and her five male children, the offspring of three different fathers, all of whom have this Syndrome. This argues for either an X linked or autosomal dominant pattern of inheritance. Cytogenetic and FISH (fluorescent in situ hybridisation) analyses were done on the mother and one son and were found to be normal.
Deepak Narayan - One of the best experts on this subject based on the ideXlab platform.
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unusual inheritance of primary ciliary Dyskinesia kartagener s Syndrome
Journal of Medical Genetics, 1994Co-Authors: Deepak Narayan, S N Krishnan, M Upender, T S Ravikumar, M J Mahoney, T F Dolan, A S Teebi, G G HaddadAbstract:Primary ciliary Dyskinesia Syndrome is characterised by chronic sinusitis, bronchiectasis, and, in 50% of cases, dextrocardia. It is generally believed to be inherited as an autosomal recessive disorder. In this report, we describe a family consisting of a mother and her five male children, the offspring of three different fathers, all of whom have this Syndrome. This argues for either an X linked or autosomal dominant pattern of inheritance. Cytogenetic and FISH (fluorescent in situ hybridisation) analyses were done on the mother and one son and were found to be normal.
S N Krishnan - One of the best experts on this subject based on the ideXlab platform.
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unusual inheritance of primary ciliary Dyskinesia kartagener s Syndrome
Journal of Medical Genetics, 1994Co-Authors: Deepak Narayan, S N Krishnan, M Upender, T S Ravikumar, M J Mahoney, T F Dolan, A S Teebi, G G HaddadAbstract:Primary ciliary Dyskinesia Syndrome is characterised by chronic sinusitis, bronchiectasis, and, in 50% of cases, dextrocardia. It is generally believed to be inherited as an autosomal recessive disorder. In this report, we describe a family consisting of a mother and her five male children, the offspring of three different fathers, all of whom have this Syndrome. This argues for either an X linked or autosomal dominant pattern of inheritance. Cytogenetic and FISH (fluorescent in situ hybridisation) analyses were done on the mother and one son and were found to be normal.
A S Teebi - One of the best experts on this subject based on the ideXlab platform.
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unusual inheritance of primary ciliary Dyskinesia kartagener s Syndrome
Journal of Medical Genetics, 1994Co-Authors: Deepak Narayan, S N Krishnan, M Upender, T S Ravikumar, M J Mahoney, T F Dolan, A S Teebi, G G HaddadAbstract:Primary ciliary Dyskinesia Syndrome is characterised by chronic sinusitis, bronchiectasis, and, in 50% of cases, dextrocardia. It is generally believed to be inherited as an autosomal recessive disorder. In this report, we describe a family consisting of a mother and her five male children, the offspring of three different fathers, all of whom have this Syndrome. This argues for either an X linked or autosomal dominant pattern of inheritance. Cytogenetic and FISH (fluorescent in situ hybridisation) analyses were done on the mother and one son and were found to be normal.
T F Dolan - One of the best experts on this subject based on the ideXlab platform.
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unusual inheritance of primary ciliary Dyskinesia kartagener s Syndrome
Journal of Medical Genetics, 1994Co-Authors: Deepak Narayan, S N Krishnan, M Upender, T S Ravikumar, M J Mahoney, T F Dolan, A S Teebi, G G HaddadAbstract:Primary ciliary Dyskinesia Syndrome is characterised by chronic sinusitis, bronchiectasis, and, in 50% of cases, dextrocardia. It is generally believed to be inherited as an autosomal recessive disorder. In this report, we describe a family consisting of a mother and her five male children, the offspring of three different fathers, all of whom have this Syndrome. This argues for either an X linked or autosomal dominant pattern of inheritance. Cytogenetic and FISH (fluorescent in situ hybridisation) analyses were done on the mother and one son and were found to be normal.