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Cytogenetic and Genome Research|August 8, 2013
Independent sex chromosome evolution in lower vertebrates: a molecular cytogenetic overview in the Erythrinidae fish familyM B Cioffi, T Liehr, V Trifonov, et al.
Oral Oncology|August 6, 1998
Oral squamous cell carcinomas are characterized by a rather uniform pattern of genomic imbalances detected by comparative genomic hybridisationE Wolff, S Girod, T Liehr, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|June 1, 1997
Isolation of DNA from the centromere of human chromosome 7 by microdissectionF Behrens, U Claussen, L M Iyer, et al.
European Journal of Human Genetics : EJHG|August 10, 1999
Maternal UPD 20 in a hyperactive child with severe growth retardationI Chudoba, Y Franke, G Senger, et al.
Genomics|February 26, 2019
Chromosomal breakpoints in a cohort of head and neck squamous cell carcinoma patientsI P Ribeiro, I M Carreira, L Esteves, et al.
Genetic Counseling (Geneva, Switzerland)|February 5, 2011
The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility?K Karaer, M A Ergun, A Weise, et al.
Human Molecular Genetics|May 1, 1995
The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instabilityA Klink, K Schiebel, M Winkelmann, et al.
Clinical Genetics|March 22, 2001
Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocationJ Seidel, S Schiller, C Kelbova, et al.
Genomics|April 1, 1993
A human pseudoautosomal gene encodes the ANT3 ADP/ATP translocase and escapes X-inactivationR Slim, J Levilliers, H J Lüdecke, et al.
Prenatal Diagnosis|July 3, 2007
Distal partial trisomy 1q: report of two cases and a review of the literatureG E Utine, D Aktas, Y Alanay, et al.
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