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American Journal of Medical Genetics

Volumn 116, Issue 1, 2003, Pages 99-100

45,X/46,XY mosaicism and fragile X syndrome [3]

(3) Banes, Shannon L a,b Begleiter, Michael L a,b Butler, Merlin G a,b

a CHILDREN S MERCY HOSPITAL (United States)

b UNIVERSITY OF MISSOURI KANSAS CITY SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; CASE REPORT; CHILD; CHROMOSOME MOSAICISM; CLINICAL FEATURE; FRAGILE X SYNDROME; GENE MUTATION; GENETIC ANALYSIS; HUMAN; KARYOTYPE 46,XY; KLINEFELTER SYNDROME; LETTER; MALE; PRIORITY JOURNAL; X CHROMOSOME;

CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, X; CHROMOSOMES, HUMAN, Y; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; HUMANS; MALE; MOSAICISM; MUTATION; NERVE TISSUE PROTEINS; RNA-BINDING PROTEINS; SEX CHROMOSOME ABERRATIONS;

EID: 0037216495 PISSN: 15524825 EISSN: None Source Type: Journal
DOI: None Document Type: Letter

Times cited : (5)

References (8)

1
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- 46,XY/47,XYY mosaicism and fragile X
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2
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- Sex chromosomal and autosomal aneuploidy in the fragile X syndrome
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- Chudley, A.¹

3
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4
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- (1988) Am J Med Genet , vol.30 , pp. 109-113
- Fryns, J.P.¹ Van den Berghe, H.²

5
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- XY/XXY mosaicism and fragile X syndrome
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6
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- Origin of the supernumerary X chromosome in a patient with fragile X and Klinefelter syndrome
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7
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8
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- Asymmetry of methylation with FMR-1 full mutation in two 45, X/46,XX mosaic females associated with normal intellect
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