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Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy
Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy
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Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy

Müller, U ; Weber, J L ; Berry, P ; Kupke, K G

Journal of medical genetics, 1993-07, Vol.30 (7), p.597-600 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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2
Multiple congenital anomalies associated with a 47,XXX chromosome constitution
Multiple congenital anomalies associated with a 47,XXX chromosome constitution
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Multiple congenital anomalies associated with a 47,XXX chromosome constitution

Hood, Opal J. ; Hartwell, Elizabeth A. ; Shattuck, Karen E. ; Rosenberg, Harvey S.

American journal of medical genetics, 1990-05, Vol.36 (1), p.73-75

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

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3
Hypothesis: The female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating x chromosome on the molecular mechanisms of neural fold elevation
Hypothesis: The female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating x chromosome on the molecular mechanisms of neural fold elevation
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Hypothesis: The female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating x chromosome on the molecular mechanisms of neural fold elevation

Juriloff, Diana M. ; Harris, Muriel J.

Birth defects research. A Clinical and molecular teratology, 2012-10, Vol.94 (10), p.849-855 [Periódico revisado por pares]

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

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4
Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay
Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay
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Familial occurrence of renal and müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay

Davee, Margaret A. ; Moore, Cynthia A. ; Bull, Marilyn J. ; Hodes, M. E.

American journal of medical genetics, 1992-10, Vol.44 (3), p.293-296

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

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