نتائج البحث

The clinical phenotype of carriers of intermediate alleles in the huntingtin gene: A scoping review

• Authors : Anna van Hofslot; Mayke Oosterloo; Joost J.A. de Jong

Subjects: Huntingtin Protein; Heterozygote; Phenotype

• Source: Journal of Huntington's Disease. 15:3-19

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Vestibular Phenotype–Genotype Correlation in a Cohort of 35 European Usher Syndrome Patients

• Authors : Ana Margarida Amorim; Ana Beatriz Ramada; Ana Cristina Lopes

Subjects: Male; Adult; Adolescent

• Source: American Journal of Audiology. 34:502-515

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New Phenotype in Two Siblings with Familial FLVCR1 Mutation: Neurotrophic Keratopathy

• Authors : Kozan, Betül Dertsiz; Alakuş, Mehmet Fuat; Polat, Hamza

Subjects: Siblings; DNA Mutational Analysis; Membrane Transport Proteins

• Source: Turk J Ophthalmol

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Survival in a Contemporary, Real-World Cohort of Patients with Mixed-Phenotype Transthyretin Amyloid Cardiomyopathy Treated with Tafamidis: An Analysis from THAOS

• Authors : Wixner J.; Dispenzieri A.; Amass L.

Subjects: Mixed phenotype; Real-world; Tafamidis

• Source: Cardiol Ther

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BCS1L‐Associated Disease: 5′‐UTR Variant Shifts the Phenotype Towards Axonal Neuropathy

• Authors : Rotem Orbach; Nunziata Maio; Russell J. Butterfield

Subjects: Male; Phenotype; Mutation, Missense

• Source: Ann Clin Transl Neurol

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REVIEW OF RESEARCH ON RECOGNITION AND MONITORING OF PLANT GROWTH PHENOTYPE BASED ON DEEP LEARNING

• Authors : Zheying ZONG; Biao FENG; Shuai WANG

• Source: INMATEH Agricultural Engineering. :81-99

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Frequency Distribution of Gingival Phenotype and its Distribution According to Tooth Shape in Patients Reporting to a Tertiary Care Dental Hospital in Lahore

• Authors : Yasir Ikram; Myra Ahmed; Farheen Qureshi

• Source: Pakistan Armed Forces Medical Journal. 75:1042-1045

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Revealing of Hormonal Characteristics of Phenotype A Polycystic Ovarian Syndrome

• Authors : null Zainab G. Falh; null Basil O. Saleh; null Afraa M. AL- Naddawi

• Source: Diyala Journal of Medicine. 29:86-96

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Pain Phenotype in Knee Osteoarthritis: Implications for Mechanism‐Based Therapy

• Authors : Chenchang He; Qiyao Li; Rui Huang

Subjects: Phenotype; Humans; Neuralgia

• Source: Orthop Surg

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Epigenome-wide analysis identifies DNA methylation signatures associated with the infant pupillary light reflex, a candidate intermediate phenotype for autism

• Authors : Fish, Laurel A.; Gliga, Teodora; Gui, Anna

Subjects: Psychiatry; Male; DNA methylation

• Source: Fish, L A, Gliga, T, Gui, A, Ali, J B, Mason, L, Johnson, M H, Charman, T, Falck-Ytter, T, Jones, E J H, Kandaswamy, R, Happé, F & Wong, C C Y 2026, 'Epigenome-wide analysis identifies DNA

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