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46,XX,inv(9)(q13q22)伴习惯性流产一例 被引量:1

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出处 《中华医学遗传学杂志》 CAS CSCD 2002年第3期204-204,共1页 Chinese Journal of Medical Genetics
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  • 1Daniely M,Aviram-Goldring A,Barkai G,et al.Detection of a chromosoma Aberration in fetuses arising from recurrent spontaneous abortion by comparative genomic hybridization[J].Hum Reprod, 1998,13 (4) : 805-809.
  • 2Magorzata Srebniak,Angelika Wawrzkiewicz,Andrzej Wiczkowski, et al.Subfertile couple with inv(2),inv(9) and 16qh+[J].J Appl Genet, 2004,45 (4) :477-479.
  • 3Kumar R,Tanwar M, Ammini A C, et al.Robertsonian translocation and their role inpatho-genesis of recurrent in vitro fertilization failure [J].Med SciMonit,2008,14( 12):617-620.
  • 4Gonul Ogurl,Elvire Van Assche,Walter Vegetti,et al.Chromosomal segregation in spermato-zoa of 4 Rpbertsonian translocation carriers[J]. HumanReproduction, 2006,12 ( 3 ) :209-215.
  • 5Nasrin Ghasemi,Seyed Mehdi Kalantar,Abbas Aflatoonian, et al. Subfertile Couples with inv(9)(p11q13):Report of two cases[J].Middle East Fertility Society Journal, 2007,12 ( 1 ):63-65.
  • 6Colls P, Blanco J,Martinez-Pasarell O,et al.Chromosome segregation in a man heterozygous for a pericentric inversion, inv ( 9 ) ( p 11 q 13 ), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization[J].Hum Genet, 1997,99 (6) :761-765.
  • 7Uccellatore F,Padova G,Squatrito S.Reproductive hormone studies in three subjects with a robertsonian translocation[J].J Endocrinol Invest, 1983,6(6):479-84.

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