Array CGH detection of a novel cryptic deletion at 3q13 in a complex chromosome rearrangement

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 ◽

Array-CGH detection of three cryptic submicroscopic imbalances in a complex chromosome rearrangement

Journal of Genetics ◽

10.1007/s12041-009-0056-4 ◽

2009 ◽

Vol 88 (3) ◽

pp. 369-372 ◽

Cited By ~ 6

Author(s):

Yanliang Zhang ◽

Yong Dai ◽

Zhiguang Tu ◽

Qiyun Li ◽

Li Zhang ◽

...

Keyword(s):

Array Cgh ◽

Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report

Molecular Cytogenetics ◽

10.1186/1755-8166-1-24 ◽

2008 ◽

Vol 1 (1) ◽

pp. 24 ◽

Cited By ~ 1

Author(s):

Emmanouil Manolakos ◽

Nadezda Kosyakova ◽

Loreta Thomaidis ◽

Rozita Neroutsou ◽

Anja Weise ◽

...

Keyword(s):

Case Report ◽

Array Cgh ◽

Terminal Deletion ◽

Facial Features ◽

Array CGH detection of a cryptic deletion in a complex chromosome rearrangement

Human Genetics ◽

10.1007/s00439-004-1248-x ◽

2005 ◽

Vol 116 (5) ◽

pp. 390-394 ◽

Cited By ~ 27

Author(s):

Carla Rosenberg ◽

Jeroen Knijnenburg ◽

Maria de Lourdes Chauffaille ◽

Decio Brunoni ◽

Ana Lucia Catelani ◽

...

Keyword(s):

Array Cgh ◽

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):

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 ◽