Results 171 to 180 of about 226,802 (259)

Phenotypic recognition of maternal (mosaic) and paternal (segmental) isodisomy for chromosome 14 without a Robertsonian translocation

open access: bronze, 2000
Sam P. Yang   +4 more
openalex   +1 more source

Association of fragile X syndrome, Robertsonian translocation (13, 22) and autism in a child. [PDF]

open access: yesClujul Med, 2017
Rachisan AL   +6 more
europepmc   +1 more source

Identification of different Robertsonian translocations in man by quinacrine mustard fluorescence analysis [PDF]

open access: gold, 2009
Torbjörn Caspersson   +4 more
openalex   +1 more source

PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization [PDF]

open access: bronze, 2011
Francesco Fiorentino   +9 more
openalex   +1 more source

The Survey of Double Robertsonian Translocation 13q; 14q in the Pedigree of 44; XX Woman: A Case Report. [PDF]

open access: yesInt J Mol Cell Med, 2017
Malekpour N   +4 more
europepmc   +1 more source

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