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Human heredity. [electronic resource].

Subjects: Medical genetics -- Periodicals; Human genetics -- Periodicals; Biometry -- Periodicals

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European journal of human genetics. [electronic resource].

• Authors : European Society of Human Genetics.

Subjects: Human genetics -- Periodicals; Medical genetics -- Periodicals; Génétique médicale -- Périodiques

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Community genetics. [electronic resource].

Subjects: Medical genetics -- Periodicals; Genetic disorders -- Diagnosis -- Periodicals; Public health -- Periodicals

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Low-Level Chromosomal Mosaicism in Neurodevelopmental Disorders

• Authors : Oneda, Beatrice; Asadollahi, Reza; Azzarello-Burri, Silvia

Subjects: Medical Clinic; Institute of Medical Genetics; 570 Life sciences

• Source: Oneda, Beatrice; Asadollahi, Reza; Azzarello-Burri, Silvia; Niedrist, Dunja; Baldinger, Rosa; Masood, Rahim; Schinzel, Albert; Latal, Bea; Jenni, Oskar G; Rauch, Anita (2017). Low-Level Chromosomal

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Personalized Nutrition

• Authors : Simopoulos, Artemis P.; Milner, John A.

Subjects: Medicine & Public Health; Nutrition; Genetics

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Personalized Nutrition : Translating Nutrigenetic/Nutrigenomic Research into Dietary Guidelines

• Authors : Simopoulos, A. P.; Milner, J. A.

Subjects: Health & Fitness / Diet & Nutrition; bisacsh:HEA048000; Medical / Genetics

• Source: MODID-00000000488:Knowledge Unlatched ; MODID-4cc7bf46c9e:KU Select 2018: STEM Backlist Books ; MODID-8d9d0ac3e3d:Karger Publishers

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Recurrent nonconvulsive status epilepticus in a patient with coffin-lowry syndrome

• Authors : Gschwind, Markus; Foletti, Giovanni; Baumer, Alessandra

Subjects: Institute of Medical Genetics; 570 Life sciences; biology

• Source: Gschwind, Markus; Foletti, Giovanni; Baumer, Alessandra; Bottani, Armand; Novy, Jan (2015). Recurrent nonconvulsive status epilepticus in a patient with coffin-lowry syndrome. Molecular Syndromology,

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Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations

• Authors : Jaureguiberry, Graciana

Subjects: Institute of Medical Genetics; 570 Life sciences; biology

• Source: Jaureguiberry, Graciana; et al (2012). Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. Nephron Physiology, 122(1-2):1-6.

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In-frame deletion and missense mutations of the C-terminal helicase domain of SMARCA2 in three patients with Nicolaides-Baraitser syndrome

• Authors : Wolff, D; Endele, S; Azzarello-Burri, S

Subjects: Medical Clinic; Institute of Medical Genetics; 570 Life sciences

• Source: Wolff, D; Endele, S; Azzarello-Burri, S; Hoyer, J; Zweier, M; Schanze, I; Schmitt, B; Rauch, A; Reis, A; Zweier, C (2012). In-frame deletion and missense mutations of the C-terminal helicase domain of

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The MEF2C-related and 5q14.3q15 microdeletion syndrome

• Authors : Zweier, M; Rauch, A

Subjects: Institute of Medical Genetics; 570 Life sciences; biology

• Source: Zweier, M; Rauch, A (2012). The MEF2C-related and 5q14.3q15 microdeletion syndrome. Molecular Syndromology, 2(3-5):164-170.

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