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  • 1-10 ل  27 نتائج ل ""Adolescent""

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Publication : bmc medical genetics Publisher : biomed central Publisher : biomed central Publisher : bmc endocrine disorders Subject : depression Subject : depression Subject : female Subject : female Subject : male Subject : male Subject : mental health Subject : mental health Subject : rasch models فلترة بواسطة : موضوع
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Identification of novel L2HGDH mutation in a large consanguineous Pakistani family- a case report

Subjects: lcsh:Internal medicine; lcsh:QH426-470; Adolescent

  • Source: BMC Medical GeneticsBMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)

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Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters

Subjects: 0301 basic medicine; Adult; lcsh:Internal medicine

  • Source: BMC Medical GeneticsBMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)

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Renin-angiotensin system gene polymorphisms and high blood pressure in Lithuanian children and adolescents

Subjects: Male; Genotyping Techniques; Cross-sectional study

  • Source: BMC Medical GeneticsBMC Medical Genetics, Vol 18, Iss 1, Pp 1-9 (2017)

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SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures

Subjects: 0301 basic medicine; Pediatrics; Family cases

  • Source: BMC Medical GeneticsBMC Medical Genetics, Vol 18, Iss 1, Pp 1-10 (2017)

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f-treeGC: a questionnaire-based family tree-creation software for genetic counseling and genome cohort studies

Subjects: 0301 basic medicine; Proband; Male

  • Source: BMC Medical GeneticsBMC Medical Genetics, Vol 18, Iss 1, Pp 1-12 (2017)

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A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2

Subjects: 0301 basic medicine; Male; DNA Mutational Analysis

  • Source: BMC Medical Genetics

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DNA methylation profiles of elderly individuals subjected to indentured childhood labor and trauma

Subjects: 0301 basic medicine; Child abuse; Male

  • Source: BMC Medical GeneticsMarinova, Z, Maercker, A, Küffer, A, Robinson, M D, Wojdacz, T K, Walitza, S, Grünblatt, E & Burri, A 2017, ' DNA methylation profiles of

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A novel mutation in the STK11 gene causes heritable Peutz-Jeghers syndrome - a case report

Subjects: 0301 basic medicine; Male; congenital, hereditary, and neonatal diseases and abnormalities

  • Source: BMC Medical Genetics

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Academic Journal

SLC1A3 C3590T but not BDNF G196A is a predisposition factor for stress as well as depression, in an adolescent eastern Indian population.

  • Authors : Ghosh M; Cytogenetics Laboratory, Department of Zoology, Banaras Hindu University, Varanasi, 221005, India.; Ali A

Subjects: Polymorphism, Single Nucleotide*; Brain-Derived Neurotrophic Factor/Brain-Derived Neurotrophic Factor/Brain-Derived Neurotrophic Factor/*genetics ; Depression/Depression/Depression/*genetics

  • Source: BMC medical genetics [BMC Med Genet] 2020 Mar 14; Vol. 21 (1), pp. 53. Date of Electronic Publication: 2020 Mar 14.Publisher: BioMed Central Country of Publication: England NLM ID: 100968552 Publication Model: Electronic Cited Medium:

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Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature

Subjects: 0301 basic medicine; Male; Pediatrics

  • Source: BMC Medical Genetics

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  • 1-10 ل  27 نتائج ل ""Adolescent""