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Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome.
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- Clinical Genetics, 1997, v. 51, n. 3, p. 184, doi. 10.1111/j.1399-0004.1997.tb02450.x
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- Article
Mythological figures in art and genetics: Current perspectives on cyclopia and chimerism.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2021, v. 187, n. 2, p. 235, doi. 10.1002/ajmg.c.31893
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- Article
Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.
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- Nature Genetics, 2002, v. 31, n. 2, p. 166, doi. 10.1038/ng889
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- Article
Genetic and epigenetic risks of intracytoplasmic sperm injection method.
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- Asian Journal of Andrology, 2006, v. 8, n. 6, p. 643, doi. 10.1111/j.1745-7262.2006.00231.x
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- Article
Nasal eosinophilia as a preliminary discriminative biomarker of non-allergic rhinitis in every day clinical pediatric practice.
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- European Archives of Oto-Rhino-Laryngology, 2023, v. 280, n. 4, p. 1775, doi. 10.1007/s00405-022-07704-0
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- Article
Developmental Dyslexia: Insights from EEG-Based Findings and Molecular Signatures—A Pilot Study.
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- Brain Sciences (2076-3425), 2024, v. 14, n. 2, p. 139, doi. 10.3390/brainsci14020139
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- Article
Developmental Dyslexia: Environment Matters.
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- Brain Sciences (2076-3425), 2021, v. 11, n. 6, p. 782, doi. 10.3390/brainsci11060782
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- Article
The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2.
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- European Journal of Human Genetics, 2014, v. 22, n. 3, p. 338, doi. 10.1038/ejhg.2013.147
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- Article
Linking Early Life Hypothalamic–Pituitary–Adrenal Axis Functioning, Brain Asymmetries, and Personality Traits in Dyslexia: An Informative Case Study.
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- Frontiers in Human Neuroscience, 2019, p. 1, doi. 10.3389/fnhum.2019.00327
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- Article
Promoter Hypermethylation of the MEG3 (DLK1/MEG3) Imprinted Gene in Multiple Myeloma.
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- Clinical Lymphoma & Myeloma, 2008, v. 8, n. 3, p. 171
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- Publication type:
- Article
Infertility and Multiple Urogenital Abnormalities in a Male with Mosaic 46,XY/45,XO/47,XXY Karyotype and Mixed Phenotype.
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- Urologia Internationalis, 1998, v. 61, n. 2, p. 111, doi. 10.1159/000030299
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- Article
Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization.
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- Molecular Medicine Reports, 2017, v. 16, n. 6, p. 8808, doi. 10.3892/mmr.2017.7760
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- Publication type:
- Article
Influence of conception and delivery mode on stress response marker Oct4B1 and imprinted gene expression related to embryo development: A cohort study.
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- International Journal of Reproductive Biomedicine, 2021, v. 19, n. 3, p. 217, doi. 10.18502/ijrm.v19i3.8569
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- Article
In-utero stress and mode of conception: impact on regulation of imprinted genes, fetal development and future health.
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- 2019
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- Publication type:
- journal article
Variation in the number of FMRI microsatellite repeats in three subgroups of the Hellenic population
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- Human Biology, 1998, v. 70, n. 3, p. 621
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- Publication type:
- Article
Mosaic Trisomy r(14) Associated With Epilepsy and Mental Retardation.
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- Journal of Child Neurology, 2007, v. 22, n. 7, p. 869, doi. 10.1177/0883073807304196
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- Publication type:
- Article
Unraveling the Serum Metabolomic Profile of Post-partum Depression.
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- Frontiers in Neuroscience, 2019, p. 1, doi. 10.3389/fnins.2019.00833
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- Publication type:
- Article
The absence of CDKN1C (p57KIP2) promoter methylation in myeloid malignancies also characterizes plasma cell neoplasms.
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- 2008
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- Publication type:
- Letter
Calcium-Sensing Receptor Gene Polymorphisms and Idiopathic Hypercalciuria in Children.
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- 2021
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- Publication type:
- Letter
Allelic imbalance of expression and epigenetic regulation within the alpha-synuclein wild-type and p.Ala53Thr alleles in Parkinson disease.
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- Human Mutation, 2010, v. 31, n. 6, p. 685, doi. 10.1002/humu.21248
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- Publication type:
- Article
Stressful Newborn Memories: Pre-Conceptual, In Utero , and Postnatal Events.
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- Frontiers in Psychiatry, 2019, p. N.PAG, doi. 10.3389/fpsyt.2019.00220
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- Publication type:
- Article
Retrotransposon RNA expression and evidence for retrotransposition events in human oocytes.
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- Human Molecular Genetics, 2009, v. 18, n. 7, p. 1221, doi. 10.1093/hmg/ddp022
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- Publication type:
- Article
An Interstitial 4q31.21q31.22 Microdeletion Associated with Developmental Delay: Case Report and Literature Review.
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- Cytogenetic & Genome Research, 2014, v. 142, n. 4, p. 227, doi. 10.1159/000361001
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- Publication type:
- Article
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.
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- Genetic Epidemiology, 1998, v. 15, n. 1, p. 103, doi. 10.1002/(SICI)1098-2272(1998)15:1<103::AID-GEPI8>3.0.CO;2-8
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- Publication type:
- Article