Download presentation
Presentation is loading. Please wait.
Published byCorey Beverly Robertson Modified over 5 years ago
1
A family with Xq22.3q25 interstitial deletion and normal ovarian function
Long-Ching Kuan, M.D., Mei-Tsz Su, M.D., Chin-Ming Wu, M.D., Ming Chen, M.D., Ph.D., Pao-Lin Kuo, M.D., Tsung-Cheng Kuo, M.D., Ph.D. Fertility and Sterility Volume 96, Issue 1, Pages e29-e34 (July 2011) DOI: /j.fertnstert Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions
2
Figure 1 (A) Karyotype of the fetus— 46,X,del(X)(q22q25). (B) Three pairs of X chromosomes in proband (a), first daughter (b), and third daughter (c) 46,X,del(X)(q22q25). (C) The pedigree of this family. The proband (I-2), her first daughter (II-1), the third daughter (fetus) (II-3) had the same chromosomal abnormality. Fertility and Sterility , e29-e34DOI: ( /j.fertnstert ) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions
3
Figure 2 (A) One copy deletion in chromosome Xq22.3q25 in the proband. (B) One copy deletion in chromosome Xq22.3q25 in the first daughter. Fertility and Sterility , e29-e34DOI: ( /j.fertnstert ) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions
4
Figure 2 (A) One copy deletion in chromosome Xq22.3q25 in the proband. (B) One copy deletion in chromosome Xq22.3q25 in the first daughter. Fertility and Sterility , e29-e34DOI: ( /j.fertnstert ) Copyright © 2011 American Society for Reproductive Medicine Terms and Conditions
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.