A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences

Reproductive Consequences ◽

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 ◽

Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24

Fertility and Sterility ◽

10.1016/j.fertnstert.2004.05.085 ◽

2004 ◽

Vol 82 (6) ◽

pp. 1666-1671 ◽

Cited By ~ 3

Author(s):

Cristina Hernando ◽

Alberto Plaja ◽

Vicens Català ◽

Enric Sarret ◽

Josep Egozcue ◽

...

Keyword(s):

Primary Amenorrhea ◽

Critical Regions ◽

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 ◽

Fluorescence In Situ Hybridization ◽

De Novo ◽

Amniotic Fluid Cells ◽

What Is a Complex Chromosome Rearrangement?

American Journal of Medical Genetics Part A ◽

10.1002/ajmg.a.35834 ◽

2013 ◽

Vol 161 (5) ◽

pp. 1181-1184 ◽

Cited By ~ 11

Author(s):

Kamlesh Madan

Keyword(s):

Prenatal diagnosis of del(4)(q27q31.23), due to a maternal balanced complex chromosome rearrangement, characterized by array-CGH

Prenatal Diagnosis ◽

10.1002/pd.2439 ◽

2010 ◽

Vol 30 (3) ◽

pp. 280-283 ◽

Cited By ~ 1

Author(s):

Francesca Malvestiti ◽

Simona De Toffol ◽

Sara Chinetti ◽

Beatrice Grimi ◽

Giancarlo Favero ◽

...

Keyword(s):

Prenatal Diagnosis ◽

Array Cgh ◽

Kallmann syndrome associated with complex chromosome rearrangement

American Journal of Medical Genetics ◽

10.1002/ajmg.1320450502 ◽

1993 ◽

Vol 45 (5) ◽

pp. 539-541 ◽

Cited By ~ 12

Author(s):

Anthony C. Casamassima ◽

Patrick L. Wilmot ◽

Betsy K. Vibert ◽

Lawrence R. Shapiro

Keyword(s):

Kallmann Syndrome ◽

A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia

European Journal of Medical Genetics ◽

10.1016/j.ejmg.2011.03.011 ◽

2011 ◽

Vol 54 (4) ◽

pp. e394-e398 ◽

Cited By ~ 4

Author(s):

Jill K. Northup ◽

Reuben Matalon ◽

Lillian H. Lockhart ◽

Judy C. Hawkins ◽

Gopalrao V.N. Velagaleti

Keyword(s):

Cleidocranial Dysplasia ◽

A 14-Year Follow-Up of a Case Detected Prenatally of Partial Trisomy 13q21.32-qter and Monosomy 18q22.3-qter as a Result of a Maternal Complex Chromosome Rearrangement Involving Chromosomes 6, 13, and 18

Genetic Testing and Molecular Biomarkers ◽

10.1089/gtmb.2008.0120 ◽

2009 ◽

Vol 13 (3) ◽

pp. 387-393 ◽

Cited By ~ 1

Author(s):

Roberto Quadrelli ◽

Andrea Quadrelli ◽

Aubrey Milunsky ◽

Ying S. Zou ◽

Xin-Li Huang ◽

...

Keyword(s):

Partial Trisomy ◽

A Girl with Pervasive Developmental Disorder and Complex Chromosome Rearrangement Involving 8p and 10p

Journal of Autism and Developmental Disorders ◽

10.1007/s10803-005-3307-0 ◽

2005 ◽

Vol 35 (3) ◽

pp. 393-399 ◽

Cited By ~ 8

Author(s):

L. Zwaigenbaum ◽

L. K. Sonnenberg ◽

T. Heshka ◽

S. Eastwood ◽

J. Xu

Keyword(s):

Pervasive Developmental Disorder ◽

Developmental Disorder ◽

Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndrome

American Journal of Medical Genetics ◽

10.1002/1096-8628(20001218)95:5<510::aid-ajmg18>3.0.co;2-v ◽

2000 ◽

Vol 95 (5) ◽

pp. 510-512

Author(s):

Andreas Zankl ◽

Marie-Claude Addor ◽

Anne-Claude Gaide ◽

Francine Thonney ◽

Pascal Cousin ◽

...

Keyword(s):

Incomplete Form ◽