Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis

De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells

American Journal of Medical Genetics ◽

10.1002/(sici)1096-8628(19980203)75:4<414::aid-ajmg12>3.0.co;2-r ◽

1998 ◽

Vol 75 (4) ◽

pp. 414-415 ◽

Cited By ~ 3

Author(s):

G. Calabrese ◽

E. Morizio ◽

P. Guanciali Franchi ◽

L. Stuppia ◽

G. Palka ◽

...

Keyword(s):

In Situ Hybridization ◽

Amniotic Fluid ◽

De Novo ◽

Amniotic Fluid Cells ◽

Premature ovarian failure in a patient with a complex chromosome rearrangement involving the critical region Xq24, characterized by analysis using fluorescence in situ hybridization by chromosome microdissection

Fertility and Sterility ◽

10.1016/j.fertnstert.2007.01.098 ◽

2007 ◽

Vol 88 (6) ◽

pp. 1677.e9-1677.e13 ◽

Cited By ~ 1

Author(s):

Jörg Weimer ◽

Subramaniyam Shivakumar ◽

Sumita Danda ◽

Nihal Thomas ◽

Laia Pagerolls Ralui ◽

...

Keyword(s):

In Situ Hybridization ◽

Premature Ovarian Failure ◽

Critical Region ◽

Ovarian Failure ◽

Chromosome Microdissection ◽

A complex chromosome rearrangement with at least five breakpoints studied by fluorescence in situ hybridization

American Journal of Medical Genetics ◽

10.1002/(sici)1096-8628(19970211)68:4<417::aid-ajmg9>3.0.co;2-i ◽

1997 ◽

Vol 68 (4) ◽

pp. 417-420 ◽

Cited By ~ 10

Author(s):

Lisa H. Gibson ◽

James McGrath ◽

Teresa L. Yang-Feng

Keyword(s):

In Situ Hybridization ◽

Complex chromosome rearrangement involving chromosomes 1, 4 and 16 revealed by fluorescence in situ hybridization

Clinical Genetics ◽

10.1111/j.1399-0004.1997.tb02472.x ◽

2008 ◽

Vol 51 (4) ◽

pp. 281-285 ◽

Cited By ~ 6

Author(s):

T. Johannesson ◽

S. Ehlers ◽

J. Wahlström

Keyword(s):

In Situ Hybridization ◽

Prenatal Diagnosis by Fluorescence in situ Hybridization on Chorionic Villus Cells: Nonsignif icance of Maternal Cell Contamination

Fetal Diagnosis and Therapy ◽

10.1159/000263910 ◽

1994 ◽

Vol 9 (2) ◽

pp. 73-76 ◽

Cited By ~ 5

Author(s):

Thue Bryndorf ◽

Britta Christensen ◽

Yang Xiang ◽

John Philip

Keyword(s):

In Situ Hybridization ◽

Prenatal Diagnosis ◽

Chorionic Villus ◽

Maternal Cell

Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples

Acta Obstetricia Et Gynecologica Scandinavica ◽

10.1080/j.1600-0412.2000.079001008.x ◽

2000 ◽

Vol 79 (1) ◽

pp. 8-14 ◽

Cited By ~ 19

Author(s):

THUE BRYNDORF ◽

CLAES LUNDSTEEN ◽

ALLEN LAMB ◽

BRITTA CHRISTENSEN ◽

JOHN PHILIP

Keyword(s):

In Situ Hybridization ◽

Prenatal Diagnosis ◽

High Risk ◽

Clinical Experience ◽

One Year

A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotyping

Annales de Génétique ◽

10.1016/s0003-3995(01)01077-2 ◽

2001 ◽

Vol 44 (3) ◽

pp. 135-138 ◽

Cited By ~ 6

Author(s):

D Kotzot ◽

H Holland ◽

M Köhler ◽

U.G Froster

Keyword(s):

In Situ Hybridisation ◽

Chromosome 8 ◽

Fluorescence In Situ Hybridisation ◽

Spectral Karyotyping ◽

Fluorescence in-situ Hybridization (FISH) in Prenatal Diagnosis: A Rapid and Reliable Tool Aiding Clinical Diagnosis

Preventive Genetics ◽

10.5005/jp/books/10670_14 ◽

2006 ◽

pp. 293-293

Author(s):

Leena Gole

Keyword(s):

In Situ Hybridization ◽

Prenatal Diagnosis ◽

Clinical Diagnosis ◽

Reliable Tool

Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies

Journal of Human Genetics ◽

10.1007/s100380050115 ◽

1999 ◽

Vol 44 (2) ◽

pp. 85-90 ◽

Cited By ~ 15

Author(s):

Keiko Wakui ◽

Mitsuyo Tanemura ◽

Kaoru Suzumori ◽

Eiko Hidaka ◽

Masayo Ishikawa ◽

...

Keyword(s):

In Situ Hybridization ◽

Prenatal Diagnosis ◽

Congenital Anomalies ◽

Chromosomal Translocation ◽

Clinical Applications ◽

Multiple Congenital Anomalies ◽

Recurrent Miscarriages

Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization

Cytogenetic and Genome Research ◽

10.1159/000134518 ◽

1997 ◽

Vol 76 (1-2) ◽

pp. 68-71 ◽

Cited By ~ 18

Author(s):

B. Levy ◽

I.F. Gershin ◽

R.J. Desnick ◽

A. Babu ◽

B.D. Gelb ◽

...

Keyword(s):

In Situ Hybridization ◽

Comparative Genomic Hybridization ◽

De Novo ◽

Comparative Genomic ◽

Genomic Hybridization