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Year | Number of Results |
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2015 | 1 |
2020 | 1 |
2021 | 2 |
2024 | 0 |
PubMed (cited) for id: 619326
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BDV Syndrome: An Emerging Syndrome With Profound Obesity and Neurodevelopmental Delay Resembling Prader-Willi Syndrome.
J Clin Endocrinol Metab. 2021 Nov 19;106(12):3413-3427. doi: 10.1210/clinem/dgab592.
J Clin Endocrinol Metab. 2021.
PMID: 34383079
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogonadism.
Durmaz A, Aykut A, Atik T, Özen S, Ayyıldız Emecen D, Ata A, Işık E, Gökşen D, Çoğulu Ö, Özkınay F.
Durmaz A, et al.
J Clin Res Pediatr Endocrinol. 2021 Feb 26;13(1):52-60. doi: 10.4274/jcrpe.galenos.2020.2020.0101. Epub 2020 Sep 17.
J Clin Res Pediatr Endocrinol. 2021.
PMID: 32936766
Free PMC article.
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Truncating Homozygous Mutation of Carboxypeptidase E (CPE) in a Morbidly Obese Female with Type 2 Diabetes Mellitus, Intellectual Disability and Hypogonadotrophic Hypogonadism.
Alsters SI, Goldstone AP, Buxton JL, Zekavati A, Sosinsky A, Yiorkas AM, Holder S, Klaber RE, Bridges N, van Haelst MM, le Roux CW, Walley AJ, Walters RG, Mueller M, Blakemore AI.
Alsters SI, et al.
PLoS One. 2015 Jun 29;10(6):e0131417. doi: 10.1371/journal.pone.0131417. eCollection 2015.
PLoS One. 2015.
PMID: 26120850
Free PMC article.
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