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1
Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes
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Reduced size of the amygdala in individuals with 47,XXY and 47,XXX karyotypes

Patwardhan, Anil J. ; Brown, Wendy E. ; Bender, Bruce G. ; Linden, Mary G. ; Eliez, Stephan ; Reiss, Allan L.

American journal of medical genetics, 2002-01, Vol.114 (1), p.93-98 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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2
Trisomy 8 mosaicism in a patient born to a mother with 47,XXX
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Trisomy 8 mosaicism in a patient born to a mother with 47,XXX

Nucaro, Anna Lisa ; Cao, Antonio ; Faedda, Antonella ; Crisponi, Giangiorgio

American journal of medical genetics, 2003-05, Vol.119A (1), p.85-86 [Periódico revisado por pares]

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

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3
Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patients
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Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patients

Lin, Henry J. ; Ndiforchu, Fombe ; Patell, Shibani

American journal of medical genetics, 1993-03, Vol.45 (6), p.761-763

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

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4
An infant with double trisomy (48,XXX, + 18)
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An infant with double trisomy (48,XXX, + 18)

Jaruratanasirikul, Somchit ; Jinorose, Uraiwan

American Journal of Medical Genetics, 1994-01, Vol.49 (2), p.207-210

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

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5
47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformation
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47,XXX chromosome constitution, ovarian dysgenesis, and genito-urinary malformation

Spear, Gerald S. ; Porto, Manuel ; Optiz, John M. ; Reynolds, James F.

American journal of medical genetics, 1988-03, Vol.29 (3), p.511-515

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

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6
Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus
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Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus

Hogge, W. Allen ; Vick, Dan J. ; Schnatterly, Patricia A. ; MacMillan, R. Hunt

American journal of medical genetics, 1989-06, Vol.33 (2), p.242-243

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

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7
Genetic significance of skewed X-chromosome inactivation in premature ovarian failure
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Genetic significance of skewed X-chromosome inactivation in premature ovarian failure

Sato, Kazuyo ; Uehara, Shigeki ; Hashiyada, Masaki ; Nabeshima, Hiroshi ; Sugawara, Jun-ichi ; Terada, Yukihiro ; Yaegashi, Nobuo ; Okamura, Kunihiro

American journal of medical genetics, 2004-10, Vol.130A (3), p.240-244 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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8
Epidemiology of triploidy in a population-based birth defects registry, Hawaii, 1986-1999
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Epidemiology of triploidy in a population-based birth defects registry, Hawaii, 1986-1999

Forrester, Mathias B. ; Merz, Ruth D.

American journal of medical genetics, 2003-06, Vol.119A (3), p.319-323 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
Neuropsychological and functional cognitive skills of 35 unselected adults with sex chromosome abnormalities
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Neuropsychological and functional cognitive skills of 35 unselected adults with sex chromosome abnormalities

Bender, Bruce G. ; Linden, Mary G. ; Harmon, Robert J.

American journal of medical genetics, 2001-09, Vol.102 (4), p.309-313 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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10
Double trisomy
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Double trisomy

Li, Shibo ; Hassed, Susan ; Mulvihill, John J. ; Nair, Ambika K. ; Hopcus, Deborah J.

American journal of medical genetics, 2004-01, Vol.124A (1), p.96-98 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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