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Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)
Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)
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Morphology, sex steroid level and gene expression analysis in gonadal sex reversal of triploid female (XXX) rainbow trout (Oncorhynchus mykiss)

Xu, Gefeng ; Huang, Tianqing ; Jin, Xian ; Cui, Cunhe ; Li, Depeng ; Sun, Cong ; Han, Ying ; Mu, Zhenbo

Fish physiology and biochemistry, 2016-02, Vol.42 (1), p.193-202 [Peer Reviewed Journal]

Dordrecht: Springer Netherlands

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The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination
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The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination

MacDonald, M. ; Hassold, T. ; Harvey, J. ; Wang, L.H. ; Morton, N.E. ; Jacobs, P.

Human molecular genetics, 1994-08, Vol.3 (8), p.1365-1371 [Peer Reviewed Journal]

Oxford: Oxford University Press

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3
Chromosome banding in Amphibia. XXX. Karyotype aberrations in cultured fibroblast cells
Chromosome banding in Amphibia. XXX. Karyotype aberrations in cultured fibroblast cells
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Chromosome banding in Amphibia. XXX. Karyotype aberrations in cultured fibroblast cells

Schmid, M ; Steinlein, C ; Haaf, T

Cytogenetic and genome research, 2004, Vol.104 (1-4), p.277-282 [Peer Reviewed Journal]

Switzerland: S. Karger AG

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4
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX
Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX
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Reduced recombination in maternal meiosis coupled with non-disjunction at meiosis II leading to recurrent 47,XXX

Reish, Orit ; Berryman, Todd ; Cunningham, Thomas R ; Sher, Carron ; Oetting, William S

Chromosome research, 2004-01, Vol.12 (2), p.125-132 [Peer Reviewed Journal]

Netherlands: Springer Nature B.V

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5
The dermatoglyphics of a Toronto sample of children with XXY, XXYY, and XXX aneuploidies
The dermatoglyphics of a Toronto sample of children with XXY, XXYY, and XXX aneuploidies
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The dermatoglyphics of a Toronto sample of children with XXY, XXYY, and XXX aneuploidies

Hreczko, T. A. ; Sigmon, Becky A.

American journal of physical anthropology, 1980-01, Vol.52 (1), p.33-41 [Peer Reviewed Journal]

New York: Wiley Subscription Services, Inc., A Wiley Company

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Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population
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Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population

Samango-Sprouse, Carole ; Kırkızlar, Eser ; Hall, Megan P ; Lawson, Patrick ; Demko, Zachary ; Zneimer, Susan M ; Curnow, Kirsten J ; Gross, Susan ; Gropman, Andrea El-Maarri, Osman

PloS one, 2016-08, Vol.11 (8), p.e0161045-e0161045 [Peer Reviewed Journal]

United States: Public Library of Science

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7
VEGF in the lung: a role for novel isoforms
VEGF in the lung: a role for novel isoforms
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VEGF in the lung: a role for novel isoforms

Varet, Julia ; Douglas, Samantha K ; Gilmartin, Laura ; Medford, Andrew R L ; Bates, David O ; Harper, Steven J ; Millar, Ann B

American journal of physiology. Lung cellular and molecular physiology, 2010-06, Vol.298 (6), p.L768-L774 [Peer Reviewed Journal]

United States: American Physiological Society

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8
Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome
Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome
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Only a minority of sex chromosome abnormalities are detected by a national prenatal screening program for Down syndrome

Viuff, Mette Hansen ; Stochholm, Kirstine ; Uldbjerg, Niels ; Nielsen, Birgitte Bruun ; Gravholt, Claus Højbjerg

Human reproduction (Oxford), 2015-10, Vol.30 (10), p.2419-2426 [Peer Reviewed Journal]

England: Oxford University Press

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9
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders
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Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders

Oetjens, M T ; Kelly, M A ; Sturm, A C ; Martin, C L ; Ledbetter, D H

Nature communications, 2019-10, Vol.10 (1), p.4897-10, Article 4897 [Peer Reviewed Journal]

England: Nature Publishing Group

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10
The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomes
The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomes
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The use of oocyte cryopreservation for fertility preservation in patients with sex chromosome disorders: a case series describing outcomes

Martel, Rachel A. ; Blakemore, Jennifer K. ; Fino, M. Elizabeth

Journal of assisted reproduction and genetics, 2022-05, Vol.39 (5), p.1143-1153 [Peer Reviewed Journal]

New York: Springer US

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