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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Adrenal Insufficiency and AAAS[original query]
Novel polymorphisms and lack of mutations in the ACD gene in patients with ACTH resistance syndromes.
Clinical endocrinology 2007 Aug 67 (2): 168-74.
Keegan Catherine E, Hutz Janna E, Krause Andrea S, Koehler Katrin, Metherell Louise A, Boikos Sosipatros, Stergiopoulos Sotirios, Clark Adrian J L, Stratakis Constantine A, Huebner Angela, Hammer Gary
Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.
Archives of medical research 2016 Apr .
Kallabi Fakhri, Belghuith Neila, Aloulou Hajer, Kammoun Thouraya, Ghorbel Soufiane, Hajji Mouna, Gallas Syrine, Chemli Jaleleddine, Chabchoub Imen, Azzouz Hatem, Ben Chehida Amel, Sfaihi Lamia, Makni Saloua, Amouri Ali, Keskes Leila, Tebib Neji, Ben Becher Saayda, Hachicha Monjia, Kamoun Hass
Phenotype-genotype spectrum of AAA syndrome from Western India and systematic review of literature.
Endocrine connections 2017 11 6 (8): 901-913.
Patt Hiren, Koehler Katrin, Lodha Sailesh, Jadhav Swati, Yerawar Chaitanya, Huebner Angela, Thakkar Kunal, Arya Sneha, Nair Sandhya, Goroshi Manjunath, Ganesh Hosahithlu, Sarathi Vijaya, Lila Anurag, Bandgar Tushar, Shah Nali
Triple-A Syndrome in Morocco: Founder Effect, Age Estimation of the AAAS c.1331+1G>A Variant, and Implications for Genetic Diagnosis.
Molecular syndromology 2024 4 15 (2): 96-103.
Karam Yahya Belmokhtar, Imane Cherkaoui, Saida Lhousni, Mounia Elidrissi Errahhali, Manal Elidrissi Errahhali, Majida Charif, Redouane Boulouiz, Meryem Ouarzane, Aziza Elouali, Ayad Ghanam, Abdeladim Babakhouya, Maria Rkain, Noufissa Benajiba, Mohammed Bellao
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