Prenatal diagnosis of a small supernumerary, XIST-negative, mosaic ring X chromosome identified by fluorescencein situ hybridization in an abnormal male fetus

2003 ◽  
Vol 23 (2) ◽  
pp. 143-145 ◽  
Author(s):  
C. Le Caignec ◽  
M. Boceno ◽  
M. Joubert ◽  
N. Winer ◽  
F. Aubron ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
X Chromosome ◽  
Fluorescencein Situ Hybridization ◽  
Male Fetus

Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus

2006 ◽  
Vol 26 (4) ◽  
pp. 387-391 ◽  
Author(s):  
Chih-Ping Chen ◽  
Shuan-Pei Lin ◽  
Chyi-Chyang Lin ◽  
Yueh-Chun Li ◽  
Lie-Jiau Hsieh ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
X Chromosome ◽  
Male Fetus ◽  
Low Level

scholarly journals Differential DNA Methylation as a Tool for Noninvasive Prenatal Diagnosis (NIPD) of X Chromosome Aneuploidies

2010 ◽  
Vol 12 (6) ◽  
pp. 797-807 ◽  
Author(s):  
Floriana Della Ragione ◽  
Paola Mastrovito ◽  
Ciro Campanile ◽  
Anna Conti ◽  
Elisavet A. Papageorgiou ◽  
...  
Keyword(s):  
Dna Methylation ◽  
Prenatal Diagnosis ◽  
X Chromosome ◽  
Noninvasive Prenatal Diagnosis

Recombinant X chromosome in a prenatal diagnosis

2006 ◽  
Vol 112 (3-4) ◽  
pp. 337-340 ◽  
Author(s):  
C. Orellana ◽  
L. Badía ◽  
F. Martínez ◽  
J.S. Oltra ◽  
S. Monfort ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
X Chromosome

scholarly journals Prenatal Diagnosis of Osteopathia Striata with Cranial Sclerosis in a Male Fetus with a ~330kb Deletion of Xq11.1 Involving the WTX Gene

2013 ◽  
Vol 1 (1) ◽  
pp. 33-36 ◽  
Author(s):  
Patrick L. Wilson ◽  
Ashley Davis ◽  
Jean Ricci Goodman ◽  
Lauren Notley ◽  
Shibo Li ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Male Fetus ◽  
Osteopathia Striata ◽  
Cranial Sclerosis

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion

1987 ◽  
Vol 75 (3) ◽  
pp. 286-290 ◽  
Author(s):  
S. V. Hodgson ◽  
M. E. Robertson ◽  
C. N. Fear ◽  
J. Goodship ◽  
S. Malcolm ◽  
...  
Keyword(s):  
Mental Retardation ◽  
Prenatal Diagnosis ◽  
X Chromosome ◽  
Chromosome Deletion

Characterization of i(18p) in prenatal diagnosis by fluorescencein situ hybridization

1993 ◽  
Vol 13 (5) ◽  
pp. 355-361 ◽  
Author(s):  
Loh-Chung Yu ◽  
John Williams ◽  
Boris B. T. Wang ◽  
Marc Vooljs ◽  
Heinz-Ulrich G. Weier ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Fluorescencein Situ Hybridization
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