De novo complex chromosomal rearrangement of 46, XY, t (3; 16; 8) (p26; q13; q21.2) in a non-obstructive azoospermic male

De Novo ◽

A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticity

Journal of Medical Genetics ◽

10.1136/jmg.37.11.892 ◽

2000 ◽

Vol 37 (11) ◽

pp. 892-896

Author(s):

W. EMBERGER

Keyword(s):

Early Onset ◽

De Novo ◽

Molecular characterization of complex chromosomal rearrangement: First report of novel t(7;12) (q11;q22) as part of a complex karyotype in de novo AML-M2 case

Pathology - Research and Practice ◽

10.1016/j.prp.2014.08.015 ◽

2014 ◽

Vol 210 (12) ◽

pp. 1090-1094 ◽

Cited By ~ 1

Author(s):

Firoz Ahmad ◽

Rupa Dalvi ◽

Swarna Mandava ◽

Bibhu R. Das

Keyword(s):

Molecular Characterization ◽

De Novo ◽

Complex Karyotype ◽

First Report ◽

Complex Chromosomal Rearrangement ◽

De Novo Aml

Advanced paternal age and de-novo complex chromosomal rearrangement in offspring

Human Reproduction ◽

10.1093/humrep/13.7.1801 ◽

1998 ◽

Vol 13 (7) ◽

pp. 1801-1803 ◽

Cited By ~ 5

Author(s):

B. Benzacken ◽

J. P. Siffroi ◽

B. Straub ◽

C. Le Bourhis ◽

S. Sauvion ◽

...

Keyword(s):

De Novo ◽

Paternal Age ◽

Advanced Paternal Age ◽

A case of prenatal detection of a de novo unbalanced complex chromosomal rearrangement involving four chromosomes

Cytology and Genetics ◽

10.3103/s009545271605011x ◽

2016 ◽

Vol 50 (5) ◽

pp. 339-342

Author(s):

L. Y. Pylyp ◽

D. O. Mykytenko ◽

L. O. Spinenko ◽

K. V. Lavrova ◽

N. V. Verhoglyad ◽

...

Keyword(s):

De Novo ◽

Prenatal Detection ◽

A de novo 3p13 deletion induced by a complex chromosomal rearrangement combined with a pericentric inversion of chromosome, inv(3)(p13q12), and a translocation between chromosome 3 and 8, t(3;8)(q13.1;q24.2), in a child with developmental delay

Genes & Genomics ◽

10.1007/s13258-016-0470-y ◽

2016 ◽

Vol 39 (2) ◽

pp. 121-126

Author(s):

Kye Hee Cho ◽

Sung Han Shim ◽

MinYoung Kim

Keyword(s):

Developmental Delay ◽

Pericentric Inversion ◽

De Novo ◽

Chromosome 3 ◽

Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3–7p15.3, including TWIST1 gene – a case report

Ginekologia Polska ◽

10.17772/gp/1768 ◽

2014 ◽

Vol 85 (7) ◽

Cited By ~ 4

Author(s):

Diana Massalska ◽

Julia Bijok ◽

Anna Kucińska-Chahwan ◽

Aleksander Jamsheer ◽

Joanna Bogdanowicz ◽

...

Keyword(s):

Case Report ◽

Prenatal Diagnosis ◽

De Novo ◽

A de novo complex chromosomal rearrangement with nine breakpoints characterised by FISH in a boy with mild mental retardation, developmental delay, short stature and microcephaly

Clinical Genetics ◽

10.1034/j.1399-0004.1999.560113.x ◽

1999 ◽

Vol 56 (1) ◽

pp. 86-92 ◽

Cited By ~ 8

Author(s):

Christine A Joyce ◽

José Carlos Cabral de Almeida ◽

Antonio Abílio Santa Rose ◽

Patricia Correia ◽

Lúcia Moraes ◽

...

Keyword(s):

Mental Retardation ◽

Short Stature ◽

Developmental Delay ◽

De Novo ◽

Mild Mental Retardation ◽

Characterization of a de novo complex chromosomal rearrangement in a patient with cri-du-chat and trisomy 5p syndromes

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.33055 ◽

2009 ◽

Vol 149A (11) ◽

pp. 2513-2521 ◽

Cited By ~ 8

Author(s):

Ascensión Vera-Carbonell ◽

Juan Antonio Bafalliu ◽

Encarna Guillén-Navarro ◽

Ariadna Escalona ◽

María J. Ballesta-Martínez ◽

...

Keyword(s):

De Novo ◽

Erratum to: A de novo 3p13 deletion induced by a complex chromosomal rearrangement combined with a pericentric inversion of chromosome 3, inv(3)(p13q12), and a translocation between chromosome 3 and 8, t(3;8)(q13.1;q24.2), in a child with developmental delay

Genes & Genomics ◽

10.1007/s13258-016-0503-6 ◽

2016 ◽

Vol 39 (2) ◽

pp. 243-243

Author(s):

Kye Hee Cho ◽

Sung Han Shim ◽

MinYoung Kim

Keyword(s):

Developmental Delay ◽

Pericentric Inversion ◽

De Novo ◽

Chromosome 3 ◽

A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility: Case report

Human Reproduction ◽

10.1093/humrep/16.1.59 ◽

2001 ◽

Vol 16 (1) ◽

pp. 59-62 ◽

Cited By ~ 19

Author(s):

Tao Cai ◽

Ping Yu ◽

Danilo A. Tagle ◽

David Lu ◽

Yiwang Chen ◽

...

Keyword(s):

Case Report ◽

De Novo ◽

Complex Chromosomal Rearrangement ◽

Male Carrier