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Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping.

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Non-syndromic X-linked mental retardation associated with a missense mutation (P312L) in the FGD1 gene.

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Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

Human molecular genetics·1996

DNA testing and genetic counseling: truth or consequences.

Wisconsin medical journal·1994

Wisconsin consanguinity studies. II: Familial adenocarcinomatosis.

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Ceperognastat in Early Symptomatic Alzheimer Disease: A Randomized Clinical Trial.

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Evaluation of insecticide susceptibility variation in different field populations of the cabbage aphid, Brevicoryne brassicae (Hemiptera: Aphididae), to selected organophosphate insecticides.

Journal of biosciences·2026

Foliar applications of a vegetal-derived protein hydrolysate alone or in combination with calcium alleviate heat stress in lettuce by boosting leaf antioxidant activity.

Frontiers in plant science·2026

QTL mapping for leaf rust resistance in bread wheat using PBW343/W8627 RIL population.

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Fragrance in Dermatology: Revisiting Sensitization and Clinical Use.

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The CsGL3-CsERF22-CsTBH-CsMYS1 pathway governs multicellular trichome development from initiation to maturation in cucumber.

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Essential oil nanoemulsion coatings as controlled-release antimicrobial mechanism for postharvest mango preservation.

Journal of the science of food and agriculture·2026

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Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping.

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