Prenatal diagnosis of a fetus with partial monosomy 7(q34→qter) and partial trisomy 18(q21→qter)

Prenatal Diagnosis ◽

10.1002/pd.1970131013 ◽

1993 ◽

Vol 13 (10) ◽

pp. 983-988 ◽

Author(s):

E. Pluchon ◽

Y. Giovangrandi ◽

F. Labbe ◽

M. J. Le Bris ◽

M. Collet ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Partial Trisomy ◽

Partial Monosomy ◽

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Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3→pter) and Partial Monosomy 13q (13q33.3→qter) Associated With Dandy-Walker Malformation, Abnormal Skull Development and Microcephaly

Taiwanese Journal of Obstetrics and Gynecology ◽

10.1016/s1028-4559(10)60068-x ◽

2010 ◽

Vol 49 (3) ◽

pp. 320-326 ◽

Author(s):

Chih-Ping Chen ◽

Ming Chen ◽

Yi-Ning Su ◽

Fuu-Jen Tsai ◽

Schu-Rern Chern ◽

...

Keyword(s):

Prenatal Diagnosis ◽

De Novo ◽

Partial Trisomy ◽

Partial Monosomy ◽

Molecular Cytogenetic ◽

Skull Development ◽

Dandy Walker Malformation ◽

Cytogenetic Characterization ◽

Walker Malformation

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Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter)

Prenatal Diagnosis ◽

10.1002/pd.1298 ◽

2005 ◽

Vol 25 (11) ◽

pp. 1069-1071 ◽

Author(s):

Chih-Ping Chen ◽

Schu-Rern Chern ◽

Tung-Yao Chang ◽

Chen-Chi Lee ◽

Wen-Lin Chen ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Partial Trisomy ◽

Partial Monosomy

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Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)

Taiwanese Journal of Obstetrics and Gynecology ◽

10.1016/j.tjog.2016.02.015 ◽

2016 ◽

Vol 55 (2) ◽

pp. 288-292 ◽

Author(s):

Chih-Ping Chen ◽

Fung-Yu Hung ◽

Schu-Rern Chern ◽

Peih-Shan Wu ◽

Yen-Ni Chen ◽

...

Keyword(s):

Prenatal Diagnosis ◽

De Novo ◽

Partial Trisomy ◽

Partial Monosomy ◽

Molecular Cytogenetic ◽

Cytogenetic Characterization

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PRENATAL DIAGNOSIS OF PARTIAL MONOSOMY 3p AND PARTIAL TRISOMY 2p IN A FETUS ASSOCIATED WITH SHORTENING OF THE LONG BONES AND A SINGLE UMBILICAL ARTERY

Prenatal Diagnosis ◽

10.1002/(sici)1097-0223(199603)16:3<270::aid-pd836>3.0.co;2-0 ◽

1996 ◽

Vol 16 (3) ◽

pp. 270-275 ◽

Author(s):

CHIH-PING CHEN ◽

FEN-FEN LIU ◽

SHEAU-WEN JAN ◽

SHUAN-PEI LIN ◽

CHUNG-CHI LAN

Keyword(s):

Prenatal Diagnosis ◽

Umbilical Artery ◽

Partial Trisomy ◽

Single Umbilical Artery ◽

Partial Monosomy

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Partial Trisomy 16p (16p12.2→pter) and Partial Monosomy 22q (22q13.31 →qter) Presenting With Fetal Ascites and Ventriculomegaly: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization

Taiwanese Journal of Obstetrics and Gynecology ◽

10.1016/s1028-4559(10)60105-2 ◽

2010 ◽

Vol 49 (4) ◽

pp. 506-512 ◽

Author(s):

Chih-Ping Chen ◽

Yi-Ning Su ◽

Richard Shih-Hung Young ◽

Fuu-Jen Tsai ◽

Pei-Chen Wu ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Comparative Genomic Hybridization ◽

Array Comparative Genomic Hybridization ◽

Partial Trisomy ◽

Comparative Genomic ◽

Genomic Hybridization ◽

Partial Monosomy

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First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13)

Prenatal Diagnosis ◽

10.1002/pd.343 ◽

2002 ◽

Vol 22 (6) ◽

pp. 487-488 ◽

Author(s):

T. Martin-Denavit ◽

J. Attia-Sobol ◽

J. Theuil ◽

K. Abel-Lablanche ◽

D. Boggio ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Partial Trisomy ◽

Partial Monosomy

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Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly

Taiwanese Journal of Obstetrics and Gynecology ◽

10.1016/j.tjog.2012.04.017 ◽

2012 ◽

Vol 51 (2) ◽

pp. 260-265

Author(s):

Pi-Lin Sung ◽

Chia-Ming Chang ◽

Chih-Yao Chen ◽

Peng-Hui Wang ◽

Kuan-Chong Chao ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Corpus Callosum ◽

Partial Trisomy ◽

Partial Monosomy ◽

Agenesis Of Corpus Callosum

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Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold

Gene ◽

10.1016/j.gene.2012.12.051 ◽

2013 ◽

Vol 516 (1) ◽

pp. 138-142 ◽

Author(s):

Chih-Ping Chen ◽

Yi-Yung Chen ◽

Schu-Rern Chern ◽

Peih-Shan Wu ◽

Jun-Wei Su ◽

...

Keyword(s):

Prenatal Diagnosis ◽

De Novo ◽

Coarctation Of The Aorta ◽

Partial Trisomy ◽

Partial Monosomy ◽

Molecular Cytogenetic ◽

Cytogenetic Characterization

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Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints

Gene ◽

10.1016/j.gene.2012.12.052 ◽

2013 ◽

Vol 516 (1) ◽

pp. 132-137 ◽

Author(s):

Chih-Ping Chen ◽

Yao-Lung Chang ◽

Schu-Rern Chern ◽

Peih-Shan Wu ◽

Jun-Wei Su ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Partial Trisomy ◽

Partial Monosomy ◽

Paternal Origin

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Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→ter→qter)

Prenatal Diagnosis ◽

10.1002/pd.1491 ◽

2006 ◽

Vol 26 (8) ◽

pp. 757-759 ◽

Author(s):

Chih-Ping Chen ◽

Chyi-Chyang Lin ◽

Tung-Yao Chang ◽

Yueh-Chun Li ◽

Lie-Jiau Hsieh ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Partial Trisomy ◽

Partial Monosomy

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