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Refinado por: Nome da Publicação: American Journal Of Medical Genetics remover assunto: Genetics & Heredity remover xxx: xxx remover
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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
47,XXX associated with malformations
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47,XXX associated with malformations

Haverty, Carrie E. ; Lin, Angela E. ; Simpson, Ellen ; Spence, M. Anne ; Martin, Rick A.

American journal of medical genetics, 2004-02, Vol.125A (1), p.108-111 [Periódico revisado por pares]

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

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3
Turner syndrome phenotype with 47,XXX karyotype: Further investigation warranted?
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Turner syndrome phenotype with 47,XXX karyotype: Further investigation warranted?

Wallerstein, Robert ; Musen, Erica ; McCarrier, Julie ; Aisenberg, Javier ; Chartoff, Amy ; Hutcheon, R. Gordon ; Tepperberg, James ; Pappenhausen, Peter ; Griffin, Sharon

American journal of medical genetics, 2004-02, Vol.125A (1), p.106-107 [Periódico revisado por pares]

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

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4
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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5
Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation
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Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation

Hammer, Sara ; Dorrani, Naghmeh ; Hartiala, Jaana ; Stein, Stuart ; Schanen, N. Carolyn

American journal of medical genetics, 2003-10, Vol.122A (3), p.223-226 [Periódico revisado por pares]

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

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6
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 [Periódico revisado por pares]

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

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7
Double trisomy (48,XXX, + 18)
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Double trisomy (48,XXX, + 18)

Tsukahara, M. ; Fukuda, M. ; Furukawa, S. ; Kondoh, O.

American journal of medical genetics, 1994-08, Vol.52 (2), p.244-244 [Periódico revisado por pares]

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

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8
47,XXX male: A clinical and molecular study
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47,XXX male: A clinical and molecular study

Ogata, Tsutomu ; Matsuo, Mari ; Muroya, Koji ; Koyama, Yasuhiro ; Fukutani, Keiko

American journal of medical genetics, 2001-02, Vol.98 (4), p.353-356 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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9
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 [Periódico revisado por pares]

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

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10
Genetic counseling for sex chromosome abnormalities
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Genetic counseling for sex chromosome abnormalities

Linden, Mary G. ; Bender, Bruce G. ; Robinson, Arthur

American journal of medical genetics, 2002-06, Vol.110 (1), p.3-10 [Periódico revisado por pares]

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

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