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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 - 5 (of 5 Records)

Query Trace: Disease and PROP1[original query]
High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency.
Endocrine 2006 Dec 30 (3): 255-60.
Halász Zita, Toke Judit, Patócs Attila, Bertalan Rita, Tömböl Zsófia, Sallai Agnes, Hosszú Eva, Muzsnai Agota, Kovács László, Sólyom János, Fekete György, Rácz Káro
Functional SNPs within the intron 1 of the PROP1 gene contribute to combined growth hormone deficiency (CPHD).
The Journal of clinical endocrinology and metabolism 2012 Sep 97 (9): E1791-7.
Godi Michela, Mellone Simona, Tiradani Luigi, Marabese Rita, Bardelli Claudio, Salerno Mariacarolina, Prodam Flavia, Bellone Simonetta, Petri Antonella, Momigliano-Richiardi Patricia, Bona Gianni, Giordano Ma
Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism.
Clinical endocrinology 2015 1 82 (6): 876-84.
Fritez Nabila, Sobrier Marie-Laure, Iraqi Hinde, Vié-Luton Marie-Pierre, Netchine Irène, El Annas Abdessamad, Pantel Jacques, Collot Nathalie, Rose Sophie, Piterboth William, Legendre Marie, Chraibi Abdelmjid, Amselem Serge, Kadiri Abdelkrim, Hilal Lati
Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiency.
Endocrine 2019 May .
Bajuk Studen Katica, Stefanija Magdalena Avbelj, Saveanu Alexandru, Barlier Anne, Brue Thierry, Pfeifer Mari
IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency.
European journal of endocrinology 2022 10 187 (6): 787-795.
Fourneaux Rachel, Reynaud Rachel, Mougel Gregory, Castets Sarah, Bretones Patricia, Dauriat Benjamin, Edouard Thomas, Raverot Gerald, Barlier Anne, Brue Thierry, Castinetti Frederic, Saveanu Alexand
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