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

Year Number of Results
1963 2
1964 13
1965 10
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1967 8
1968 17
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1970 34
1971 42
1972 63
1973 43
1974 65
1975 43
1976 46
1977 33
1978 40
1979 25
1980 28
1981 26
1982 51
1983 44
1984 58
1985 60
1986 55
1987 48
1988 63
1989 54
1990 52
1991 44
1992 46
1993 46
1994 57
1995 59
1996 60
1997 62
1998 33
1999 54
2000 48
2001 58
2002 48
2003 50
2004 45
2005 44
2006 41
2007 44
2008 32
2009 39
2010 49
2011 65
2012 67
2013 59
2014 58
2015 51
2016 51
2017 51
2018 55
2019 64
2020 63
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2022 45
2023 48
2024 15

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2,617 results

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Quoted phrase not found in phrase index: "Anomaly of sex chromosome"
Page 1
Fetal dermatoglyphics.
Katznelson MB, Goldman B. Katznelson MB, et al. Clin Genet. 1982 Apr;21(4):237-42. doi: 10.1111/j.1399-0004.1982.tb00757.x. Clin Genet. 1982. PMID: 6213324
Dermatoglyphic studies were performed on 24 aborted human embryos in whom major chromosomal aberrations had been revealed by amniocentesis. Prints were obtained from the embryos by the Hollister method. ...The fetuses had the following disorders: 7 with trisomy 21, 2 with …
Dermatoglyphic studies were performed on 24 aborted human embryos in whom major chromosomal aberrations had been revealed by amniocen …
The XYY syndrome.
Parker CE, Melyk J, Fish CH. Parker CE, et al. Am J Med. 1969 Nov;47(5):801-8. doi: 10.1016/0002-9343(69)90173-9. Am J Med. 1969. PMID: 4901976 Review. No abstract available.
Prenatal diagnosis of sex chromosome aneuploidies: experience at a mainland Chinese hospital.
Liao C, Yi CX, Li DZ. Liao C, et al. J Obstet Gynaecol. 2013 Nov;33(8):827-9. doi: 10.3109/01443615.2013.831049. J Obstet Gynaecol. 2013. PMID: 24219724
The aim of this study is to assess the initial indications, frequency and termination rates of pregnancies with sex chromosome aneuploidies (SCAs), at a mainland Chinese hospital. ...
The aim of this study is to assess the initial indications, frequency and termination rates of pregnancies with sex chromosome …
Parents' adaptation to early diagnosis of sex chromosome anomalies.
Puck MH, Bender BG, Borelli JB, Salbenblatt JA, Robinson A. Puck MH, et al. Am J Med Genet. 1983 Sep;16(1):71-9. doi: 10.1002/ajmg.1320160112. Am J Med Genet. 1983. PMID: 6638073
In 56 structured psychiatric interviews parents were asked to describe their experience as participants in the Denver prospective study of children with sex chromosome anomalies in order to assess its impact on attitudes toward the identified child and on family rel …
In 56 structured psychiatric interviews parents were asked to describe their experience as participants in the Denver prospective study of c …
Preimplantation diagnosis of genetic and chromosomal disorders.
Verlinsky Y, Handyside A, Grifo J, Munné S, Cohen J, Liebers I, Levinson G, Arnheim N, Hughes M, Delhanty J, et al. Verlinsky Y, et al. J Assist Reprod Genet. 1994 May;11(5):236-43. doi: 10.1007/BF02214343. J Assist Reprod Genet. 1994. PMID: 7711387 Review. No abstract available.
Visualization of the fetal genitalia by ultrasonography: a review of the literature and analysis of its accuracy and ethical implications.
Elejalde BR, de Elejalde MM, Heitman T. Elejalde BR, et al. J Ultrasound Med. 1985 Dec;4(12):633-9. doi: 10.7863/jum.1985.4.12.633. J Ultrasound Med. 1985. PMID: 3908716 Review.
Ultrasonographic determination of fetal gender in utero is an integral part of the prenatal diagnosis of sex maldefinition, testicular feminization, and campomelic dysplasia. It has proved to be a reliable marker in determining whether each sac has been sampled in multiple …
Ultrasonographic determination of fetal gender in utero is an integral part of the prenatal diagnosis of sex maldefinition, testicula …
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY.
Chen CP, Chern SR, Chang CL, Lee CC, Chen WL, Chen LF, Wang W. Chen CP, et al. Prenat Diagn. 2000 Sep;20(9):754-7. doi: 10.1002/1097-0223(200009)20:9<754::aid-pd896>3.0.co;2-n. Prenat Diagn. 2000. PMID: 11015707
Quantitative fluorescent polymerase chain reaction (QF-PCR) with small tandem repeat (STR) markers specific for chromosome X and a pentanucleotide marker X22 for the Xq/Yq pseudoautosomal region PAR2 rapidly detected the X-chromosome polysomy from amniotic fluid cel …
Quantitative fluorescent polymerase chain reaction (QF-PCR) with small tandem repeat (STR) markers specific for chromosome X and a pe …
Sex chromosomal anomalies in pregnancies conceived through intracytoplasmic sperm injection: a case for genetic counselling.
Meschede D, Horst J. Meschede D, et al. Hum Reprod. 1997 Jun;12(6):1125-7. doi: 10.1093/humrep/12.6.1125. Hum Reprod. 1997. PMID: 9221988 Review.
We discuss here in detail the developmental prognosis of individuals carrying a sex chromosomal anomaly. Major malformations do occur in Turner syndrome, but not so in Klinefelter, the triple X and the XYY syndromes. ...Academic achievement, however, may be somewhat …
We discuss here in detail the developmental prognosis of individuals carrying a sex chromosomal anomaly. Major malformations d …
The prenatal diagnosis of genetic disorders.
Epstein CJ, Golbus MS. Epstein CJ, et al. Annu Rev Med. 1978;29:117-28. doi: 10.1146/annurev.me.29.020178.001001. Annu Rev Med. 1978. PMID: 348029 Review.
2,617 results