SANDRA DARILEK to Humans
This is a "connection" page, showing publications SANDRA DARILEK has written about Humans.
Connection Strength
0.116
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Telegenetics to provide comprehensive prenatal diagnosis. Prenat Diagn. 2024 04; 44(4):492-498.
Score: 0.025
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Basic medical genetics for the otolaryngologist. Adv Otorhinolaryngol. 2011; 70:10-17.
Score: 0.010
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Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives. Genet Med. 2008 Jan; 10(1):13-8.
Score: 0.008
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Hereditary multiple exostosis and pain. J Pediatr Orthop. 2005 May-Jun; 25(3):369-76.
Score: 0.007
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Family Lore, a Variant of Uncertain Significance, and?CADASIL. Am J Med Genet C Semin Med Genet. 2024 Nov; 196(2-3):e32117.
Score: 0.007
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Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2023 02; 25(2):100336.
Score: 0.006
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A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature. Am J Med Genet A. 2021 10; 185(10):2903-2912.
Score: 0.005
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The sixth international RASopathies symposium: Precision medicine-From promise to practice. Am J Med Genet A. 2020 03; 182(3):597-606.
Score: 0.005
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Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum. Am J Med Genet A. 2019 03; 179(3):386-396.
Score: 0.004
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Attitudes Toward and Uptake of Prenatal Genetic Screening and Testing in Twin Pregnancies. J Genet Couns. 2018 09; 27(5):1238-1247.
Score: 0.004
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Genesurance Counseling: Patient Perspectives. J Genet Couns. 2018 08; 27(4):814-822.
Score: 0.004
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Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. J Womens Health (Larchmt). 2017 07; 26(7):755-761.
Score: 0.004
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Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO. J Med Genet. 2017 01; 54(1):47-53.
Score: 0.004
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The ethics of conducting molecular autopsies in cases of sudden death in the young. Genome Res. 2016 09; 26(9):1165-9.
Score: 0.004
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Genetic counseling for men with recurrent pregnancy loss or recurrent implantation failure due to abnormal sperm chromosomal aneuploidy. J Assist Reprod Genet. 2016 May; 33(5):571-576.
Score: 0.004
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DNA sequence analysis and genotype-phenotype assessment in 71 patients with syndromic hearing loss or auditory neuropathy. BMJ Open. 2015 May 19; 5(5):e007506.
Score: 0.003
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Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes. Fam Cancer. 2010 Sep; 9(3):479-87.
Score: 0.002
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Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenat Diagn. 2009 Jan; 29(1):29-39.
Score: 0.002
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Infrequency of two deletion mutations at the DFNB1 locus in patients and controls. Am J Med Genet A. 2008 Apr 01; 146A(7):934-6.
Score: 0.002
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DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls. Am J Med Genet A. 2006 Nov 15; 140(22):2401-15.
Score: 0.002
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Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genet Med. 2006 Nov; 8(11):719-27.
Score: 0.002
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A retrospective study of preimplantation embryos diagnosed with monosomy by fluorescence in situ hybridization (FISH). Cytogenet Genome Res. 2006; 114(3-4):359-66.
Score: 0.002