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Results 1 - 10 of 96,047  for Great Falls College MSU

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Patients with 47, XXX karyotype who experienced premature ovarian failure (POF): two case reports

Sugawara, Nobuo ; Maeda, Machiko ; Manome, Tomomi ; Nagai, Rie ; Araki, Yasuhisa

Reproductive Medicine and Biology, October 2013, Vol.12(4), pp.193-195 [Peer Reviewed Journal]

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Gilles de la Tourette's syndrome in a patient with 47(XXX) syndrome: a case report.(Case report)

Chiappedi, Matteo ; De Vincenzi, Silvia ; Dolci, Roberta ; De Luca, Sara ; Bejor, Maurizio

Journal of Medical Case Reports, Nov 5, 2011, Vol.5, p.542 [Peer Reviewed Journal]

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Gilles de la Tourette's syndrome in a patient with 47(XXX) syndrome: a case report.(Case study)

Chiappedi, Matteo ; De Vincenzi, Silvia ; Dolci, Roberta ; De Luca, Sara ; Bejor, Maurizio

Journal of Medical Case Reports, Nov 5, 2011, Vol.5, p.542 [Peer Reviewed Journal]

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Gilles de la Tourette's syndrome in a patient with 47(XXX) syndrome: a case report

Chiappedi, Matteo ; De Vincenzi, Silvia ; Dolci, Roberta ; De Luca, Sara ; Bejor, Maurizio

Journal of medical case reports, 05 November 2011, Vol.5, pp.542 [Peer Reviewed Journal]

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Generalized epilepsy in a patient with mosaic Turner syndrome: a case report

Jhang, Kai-Ming ; Chang, Tung-Ming ; Chen, Ming ; Liu, Chin-San

Journal of medical case reports, 02 April 2014, Vol.8, pp.109 [Peer Reviewed Journal]

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47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries

Rafique, Munazzah ; Alobaid, Solaiman ; Al‐Jaroudi, Dania

Clinical Case Reports, June 2019, Vol.7(6), pp.1238-1241 [Peer Reviewed Journal]

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Genetic and Clinical Features of Triploid Fetus: A Case Report in Han Chinese Population

Zhu, Jiansheng ; Liu, Hui ; Wang, Yaqun ; Khan, Muhammad ; Bukhari, Ihtisham ; Wang, Baolong

Pakistan Journal of Zoology, Apr 2015, Vol.47(2) [Peer Reviewed Journal]

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An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.

Anneren, G ; Andersson, M ; Page, D ; Brown, L ; Berg, M ; Laackgren, G ; Gustavson, K-H ; de La Chapelle, A Anneren, G (correspondence author)

American Journal of Human Genetics, 1987, Vol.41(4), pp.594-604 [Peer Reviewed Journal]

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Craniofacial and dental manifestations of triple X syndrome associated with congenital hypothyroidism: a case report

Ferrazzo, Kívia Linhares ; Payeras, Marcia Rodrigues ; Ferrazzo, Vilmar Antonio ; Mezomo, Maurício Barbieri

Special Care in Dentistry, May 2014, Vol.34(3), pp.156-159 [Peer Reviewed Journal]

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A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case report.(Case study)

Tian, Chan ; Li, Dan ; Liu, Ping ; Jiao, Liping ; Gao, Xuefeng ; Qiao, Jie

Molecular Cytogenetics, Sept 2, 2017, Vol.10(1) [Peer Reviewed Journal]

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