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1963
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1963 23
1964 39
1965 28
1966 38
1967 40
1968 57
1969 66
1970 65
1971 56
1972 88
1973 78
1974 58
1975 64
1976 50
1977 48
1978 58
1979 60
1980 46
1981 87
1982 66
1983 81
1984 71
1985 89
1986 113
1987 129
1988 152
1989 199
1990 229
1991 247
1992 310
1993 315
1994 302
1995 311
1996 307
1997 332
1998 333
1999 397
2000 414
2001 376
2002 311
2003 315
2004 342
2005 364
2006 382
2007 335
2008 316
2009 332
2010 382
2011 383
2012 370
2013 377
2014 417
2015 362
2016 403
2017 368
2018 370
2019 334
2020 354
2021 333
2022 284
2023 313
2024 271
2025 11

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13,051 results

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Page 1
Testicular cancer.
Cheng L, Albers P, Berney DM, Feldman DR, Daugaard G, Gilligan T, Looijenga LHJ. Cheng L, et al. Nat Rev Dis Primers. 2018 Oct 5;4(1):29. doi: 10.1038/s41572-018-0029-0. Nat Rev Dis Primers. 2018. PMID: 30291251 Review.
Progress has been made in our understanding of the disease since the initial description of carcinoma in situ of the testis in 1972 (now referred to as germ cell neoplasia in situ), which has led to improved treatment options. ...
Progress has been made in our understanding of the disease since the initial description of carcinoma in situ of the testis in 1972 ( …
Preimplantation Genetic Testing for Chromosomal Abnormalities: Aneuploidy, Mosaicism, and Structural Rearrangements.
Viotti M. Viotti M. Genes (Basel). 2020 May 29;11(6):602. doi: 10.3390/genes11060602. Genes (Basel). 2020. PMID: 32485954 Free PMC article. Review.
Cells with chromosomal copy number deviations or chromosome structural rearrangements can compromise the viability of embryos; much of the naturally low human fecundity as well as low success rates of ART can be ascribed to these cytogenetic defects. Chromosomal
Cells with chromosomal copy number deviations or chromosome structural rearrangements can compromise the viability of embryos; …
Imprinting disorders in humans: a review.
Butler MG. Butler MG. Curr Opin Pediatr. 2020 Dec;32(6):719-729. doi: 10.1097/MOP.0000000000000965. Curr Opin Pediatr. 2020. PMID: 33148967 Free PMC article. Review.
Many imprinted genes affect fetal growth and development accounting for several human disorders reviewed in this report. RECENT FINDINGS: Disorders include Prader-Willi and Angelman syndromes, the first examples of imprinting errors in humans, chromosome 15q1 …
Many imprinted genes affect fetal growth and development accounting for several human disorders reviewed in this report. RECENT FINDI …
Updated consensus guidelines on the management of Phelan-McDermid syndrome.
Srivastava S, Sahin M, Buxbaum JD, Berry-Kravis E, Soorya LV, Thurm A, Bernstein JA, Asante-Otoo A, Bennett WE Jr, Betancur C, Brickhouse TH, Passos Bueno MR, Chopra M, Christensen CK, Cully JL, Dies K, Friedman K, Gummere B, Holder JL Jr, Jimenez-Gomez A, Kerins CA, Khan O, Kohlenberg T, Lacro RV, Levi LA, Levy T, Linnehan D, Eva L, Moshiree B, Neumeyer A, Paul SM, Phelan K, Persico A, Rapaport R, Rogers C, Saland J, Sethuram S, Shapiro J, Tarr PI, White KM, Wickstrom J, Williams KM, Winrow D, Wishart B, Kolevzon A. Srivastava S, et al. Am J Med Genet A. 2023 Aug;191(8):2015-2044. doi: 10.1002/ajmg.a.63312. Epub 2023 Jul 1. Am J Med Genet A. 2023. PMID: 37392087 Free PMC article. Review.
Since there is limited evidence specific to PMS, intervention mostly follows general guidelines for treating individuals with developmental disorders. Significant evidence has been amassed to guide the management of comorbid neuropsychiatric conditions in PMS, albeit mainl …
Since there is limited evidence specific to PMS, intervention mostly follows general guidelines for treating individuals with developmental …
Sex chromosome aneuploidies.
Skuse D, Printzlau F, Wolstencroft J. Skuse D, et al. Handb Clin Neurol. 2018;147:355-376. doi: 10.1016/B978-0-444-63233-3.00024-5. Handb Clin Neurol. 2018. PMID: 29325624 Review.
Sex chromosome aneuploidies comprise a relatively common group of chromosome disorders characterized by the loss or gain of one or more sex chromosomes. ...The loss or gain of genetic material can affect all daughter cells or it may be partial, leading to tis …
Sex chromosome aneuploidies comprise a relatively common group of chromosome disorders characterized by the loss or gai …
Prenatal diagnosis by chromosomal microarray analysis.
Levy B, Wapner R. Levy B, et al. Fertil Steril. 2018 Feb;109(2):201-212. doi: 10.1016/j.fertnstert.2018.01.005. Fertil Steril. 2018. PMID: 29447663 Free PMC article. Review.
Chromosomal microarray analysis (CMA) is performed either by array comparative genomic hybridization or by using a single nucleotide polymorphism array. In the prenatal setting, CMA is on par with traditional karyotyping for detection of major chromosomal imbalances
Chromosomal microarray analysis (CMA) is performed either by array comparative genomic hybridization or by using a single nucleotide
Triploid pregnancy-Clinical implications.
Massalska D, Bijok J, Kucińska-Chahwan A, Zimowski JG, Ozdarska K, Panek G, Roszkowski T. Massalska D, et al. Clin Genet. 2021 Oct;100(4):368-375. doi: 10.1111/cge.14003. Epub 2021 Jun 1. Clin Genet. 2021. PMID: 34031868 Review.
48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome.
Tartaglia N, Ayari N, Howell S, D'Epagnier C, Zeitler P. Tartaglia N, et al. Acta Paediatr. 2011 Jun;100(6):851-60. doi: 10.1111/j.1651-2227.2011.02235.x. Epub 2011 Apr 8. Acta Paediatr. 2011. PMID: 21342258 Free PMC article. Review.
Sex chromosome tetrasomy and pentasomy conditions occur in 1:18,000-1:100,000 male births. While often compared with 47,XXY/Klinefelter syndrome because of shared features including tall stature and hypergonadotropic hypogonadism, 48,XXYY, 48,XXXY and 49,XXXXY syndromes ar …
Sex chromosome tetrasomy and pentasomy conditions occur in 1:18,000-1:100,000 male births. While often compared with 47,XXY/Klinefelt …
Pseudoacromegaly.
Marques P, Korbonits M. Marques P, et al. Front Neuroendocrinol. 2019 Jan;52:113-143. doi: 10.1016/j.yfrne.2018.11.001. Epub 2018 Nov 15. Front Neuroendocrinol. 2019. PMID: 30448536 Review.
13,051 results
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