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Subject 599.935

101. Bight of Benin: a Maternal Perspective of Four Beninese Populations and their Genetic Implications on the American Populations of African Ancestry. (March 2017)

Authors:
Primativo, Giuseppina; Ottoni, Claudio; Biondi, Gianfranco; Serafino, Sara; Martínez‐Labarga, Cristina; Larmuseau, Maarten H. D.; Scardi, Michele; Decorte, Ronny; Rickards, Olga
Journal:
Annals of human genetics
Issue:
Volume 81:Number 2(2017:Mar.)
Page Start:
78
Record Type:
Journal Article
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102. Biochemistry, Cytogenetics and DMD Gene Mutations in South Indian Patients with Duchenne Muscular Dystrophy. (3rd July 2017)

Authors:
Meyyazhagan, A.; Raman, N. M.; Easwaran, M.; Balasubramanian, B.; Alagamuthu, K.; Bhotla, H. Kuchi; Shanmugam, S.; Inbaraj, K.; Ramesh Kumar, M.; Kumar, P.; Thangamani, L.; Piramanayagam, S.; Anand, V.; Mohd, Y.; Park, S.; Teijido, O.; Carril, J.C.; Cacabelos, P.; Keshavarao, S.; Cacabelos, R.
Journal:
International journal of human genetics
Issue:
Volume 17:Number 3(2017)
Page Start:
126
Record Type:
Journal Article
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104. C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease. (12th July 2013)

Authors:
Nuytemans, Karen; Bademci, Güney; Kohli, Martin M.; Beecham, Gary W.; Wang, Liyong; Young, Juan I.; Nahab, Fatta; Martin, Eden R.; Gilbert, John R.; Benatar, Michael; Haines, Jonathan L.; Scott, William K.; Züchner, Stephan; Pericak‐Vance, Margaret A.; Vance, Jeffery M.
Journal:
Annals of human genetics
Issue:
Volume 77:Number 5(2013:Sep.)
Page Start:
351
Record Type:
Journal Article
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107. CFTR mutational screening by next‐generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population. (9th December 2021)

Authors:
Farra, Chantal; Awwad, Johnny; Hamadeh, Lama; Khoueiry, Pierre; Halawi, Zeina; Yazbeck, Nadine; Daher, Rose; Souaid, Mirna; Hamdar, Layal; Yammine, Tony; Yunis, Khalid
Journal:
Annals of human genetics
Issue:
Volume 86:Number 2(2022)
Page Start:
80
Record Type:
Journal Article
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108. Changes of the echocardiographic parameters in chronic heart failure patients with Ile337val, Glu23lys, and Ser1369ala polymorphisms of genes encoding the ATP‐sensitive potassium channels subunits in the Ukrainian population. (13th July 2018)

Authors:
Strutynskyi, R. B.; Voronkov, L. G.; Nagibin, V. S.; Mazur, I. D.; Stroy, D.; Dosenko, V. E.
Journal:
Annals of human genetics
Issue:
Volume 82:Number 5(2018:Sep.)
Page Start:
272
Record Type:
Journal Article
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109. Charcot‐Marie‐Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families. (24th September 2015)

Authors:
Hyun, Young Se; Lee, Jinho; Kim, Hye Jin; Hong, Young Bin; Koo, Heasoo; Smith, Alec S.T.; Kim, Deok‐Ho; Choi, Byung‐Ok; Chung, Ki Wha
Journal:
Annals of human genetics
Issue:
Volume 79:Number 6(2015:Nov.)
Page Start:
460
Record Type:
Journal Article
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