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Scholar Results 1 - 9 of 9 citing Yorifuji: Analysis of the SRY gene in Turner syndrome patients with Y chromosomal material. (0.06 sec) 

Three new novel point mutations localized within and downstream of high-mobility group- …

- endojournals.org
M Shahid, VS Dhillon, M Aslam, SA Husain - Journal of Clinical Endocrinology & Metabolism, 2005 - Endocrine Soc
Point mutations and deletions in the SRY gene result in XY sex reversal in pure
gonadal dysgenesis. To date, a majority of these affect the high-mobility group
(HMG) domain of SRY, which plays a key role in its DNA binding activity. We ...
Cited by 13 - Related articles - All 4 versions

Three new novel point mutations localized within and downstream of HMG-box region in SRY …

- endojournals.org [PDF] 
M Shahid, VS Dhillon, M Aslam, SA Husain - Journal of Clinical Endocrinology & Metabolism, 2005 - Endocrine Soc
1 Human Genetics Lab, Department of Biosciences, Jamia Millia Islamia, New
Delhi-110 025, INDIA, 2 CSIRO Health Sciences and Nutrition, PO Box 10041,
Adelaide BC, Adelaide 5000, Australia ... Dr Varinderpal S Dhillon Genome ...
Cited by 1 - Related articles

Analysis of the SRY gene in Turner syndrome patients from the Republic of Macedonia

- bjmg.edu.mk [PDF] 
A Papazovska-Cherepnalkovski, S Koceva, M … - Balkan Journal of Medical Genetics, 2008 - Versita
*Corresponding Author: Mirjana Kocova, MD, Ph.D., Department of Endocrinology
and Genetics, University Pediatric Clinic, Vodnjanska 17, 1000 Skopje, Republic
of Macedonia; Tel.: +389-2-3147-474/+389-70-242-694; Fax: +389-2-3129-027; ...
Cited by 1 - Related articles - All 2 versions

Paternally derived der (7) t (Y; 7)(p11. 1∼ 11.2; p22. 3) dn in a mosaic case with Turner …


AD Polityko, OM Khurs, AI Kulpanovich, KA … - European Journal of Medical Genetics, 2009 - Elsevier
An unusual mosaic karyotype was detected in a 6-year-old female patient with
clinical diagnosis of Turner syndrome (TS). Cytogenetic and molecular
cytogenetic studies revealed besides a cell line with 45,X a second cell ...
Related articles - All 2 versions

Journal List> Korean J Lab Med> v. 26 (2); Apr 2006


HR Kim, JH Shin, WY Jung, JN Lee - Korean J Lab Med, 2006 - synapse.koreamed.org
Korean J Lab Med. 2006 Apr;26(2):131-136. Published online 2006 April 20. doi:
10.3343/kjlm.2006.26.2.131. ... 1 Department of Laboratory Medicine, Busan Paik
Hospital, College of Medicine, Inje University, Busan, Korea.
Related articles - Cached

Les chromosomes Y dicentriques


NB Abdelmoula, A Amouri - Ann Biol Clin, 2005 - john-libbey-eurotext.fr
Résumé : Les chromosomes dicentriques sont parmi les anomalies de structure
les plus fréquentes du chromosome Y. La prédiction de leurs conséquences
phénotypiques est souvent difficile du fait de : 1) la diversité des ...
Related articles - All 2 versions

[PDF] Turner 증후군 환자에서 분자유전학적 방법을 이용한 Y 염색체의 증명


김혜란, 신정환, 정우영, 이정녀, 결론, 모든 - 대한진단검사의학회지, 2006 - kslm.org
Turner가 처음으로 성적 영아증(sexual infantilism), 익상경(web neck)
및 외반주(cubitus valgus)와 난소부전을 특징으로 하는 일련의
증후군을 발표하였으며, 1959년 Ford가 처음으로 세포유 ...
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Dicentric Y chromosomes: first part: cytogenetic and molecular aspects.


PDF Version - john-libbey-eurotext.fr
Summary : Dicentric Y chromosomes have been reviewed twice in 1994 by Hsu et al.
and in 1995 by Tuck-Muller et al. who showed that dic(Y) are the most common Y
structural abnormalities and that their influence on gonadal and somatic ...
Related articles - All 2 versions

[PDF] Turner 증후군 환자에서 분자유전학적 방법을 이용한 Y 염색체의 증명


HR Kim, JH Shin, WY Jung, JN Lee - 대한진단검사의학회지, 2006 - synapse.koreamed.org
Turner가 처음으로 성적 영아증(sexual infantilism), 익상경(web neck)
및 외반주(cubitus valgus)와 난소부전을 특징으로 하는 일련의
증후군을 발표하였으며, 1959년 Ford가 처음으로 세포유 ...
Related articles - View as HTML - All 2 versions


 


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