A genetic marker of the ACKR1 gene is present in patients with Type II congenital smell loss who have type I hyposmia and hypogeusia.

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A genetic marker of the ACKR1 gene is present in patients with Type II congenital smell loss who have type I hyposmia and hypogeusia.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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A genetic marker of the ACKR1 ...... ype I hyposmia and hypogeusia.

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A genetic marker of the ACKR1 ...... ype I hyposmia and hypogeusia.

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type

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A genetic marker of the ACKR1 ...... ype I hyposmia and hypogeusia.

@en

A genetic marker of the ACKR1 ...... ype I hyposmia and hypogeusia.

@nl

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A genetic marker of the ACKR1 ...... ype I hyposmia and hypogeusia.

@en

A genetic marker of the ACKR1 ...... ype I hyposmia and hypogeusia.

@nl

P1476

A genetic marker of the ACKR1 ...... type I hyposmia and hypogeusia

@en

P2093

Robert I Henkin

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William A Stateman

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Willy A Flegel

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P2860

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism

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Functional MRI of congenital hyposmia: brain activation to odors and imagination of odors and tastes.

Erythrocyte membrane antigen frequencies in patients with Type II congenital smell loss.

The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome.

International Union of Basic and Clinical Pharmacology. [corrected]. LXXXIX. Update on the extended family of chemokine receptors and introducing a new nomenclature for atypical chemokine receptors.

Identification of HESX1 mutations in Kallmann syndrome.

Applying molecular immunohaematology to regularly transfused thalassaemic patients in Thailand.

Taste and smell function in chronic disease: a review of clinical and biochemical evaluations of taste and smell dysfunction in over 5000 patients at The Taste and Smell Clinic in Washington, DC.

Anatomic olfactory structural abnormalities in congenital smell loss: magnetic resonance imaging evaluation of olfactory bulb, groove, sulcal, and hippocampal morphology.

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484-489

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scholarly article

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10.1016/J.AMJOTO.2015.07.006

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P433

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P478

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Alexandra B Knöppel

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2015-07-15T00:00:00Z

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P698

27968956

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P921

Hyposmia

birth defect

P932

5159426

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