Results 61 to 70 of about 24,048 (165)

Single Nucleotide Polymorphism Microarray Analysis Unveils Copy-Number Abnormalities and Genetic Heterogeneity in Malaysian Childhood B-Cell Precursor Acute Lymphoblastic Leukemia. [PDF]

Mol Genet Genomic Med
Mohd Dali NS, Aziz NA, Zulkifle MF, Zamri DA, Kamaluddin NR, Yeoh SL, Ho BL, Din ND, Ab Ghani AS, Wan Hassan WAH, Zakaria Z, Esa E, Mat Yusoff Y.   +12 more
europepmc   +1 more source

Intrachromosomal insertion as a diagnostic challenge: a hidden structural rearrangement causing recurrent duplication and deletion. [PDF]

Mol Cytogenet
Kawamura R, Shichiri Y, Suzuki H, Murase Y, Naru Y, Hara T, Tsuboi A, Satano H, Sugihara E, Kurahashi H.   +9 more
europepmc   +1 more source

Chromosome Banding [PDF]

Journal of Medical Genetics, 1991
openaire   +1 more source

<i>Chironomus</i> sp. J - an elusive species from the <i>Chironomus plumosus</i> (Linnaeus, 1758) sibling-species group (Diptera, Chironomidae). [PDF]

Comp Cytogenet
Golygina VV.
europepmc   +1 more source

An intraspecific origin of B chromosomes in Tetragonisca fiebrigi (Apidae: Meliponini) inferred from cytogenetic and nuclear genome size data. [PDF]

Sci Rep
Cunha MS, Lino-Neto J, Soares FAF, Clarindo WR, Rönnau M, Campos LAO, Lopes DM.   +6 more
europepmc   +1 more source

Chromosome Band [PDF]

, 2020
openaire   +1 more source

Impact of chromosomal polymorphisms on pregnancy outcomes after in vitro fertilization or intracytoplasmic sperm injection: A systematic review and meta-analysis. [PDF]

Pak J Med Sci
Shen L, Sun Q, Shen L, Zhu Y, Sun Y.
europepmc   +1 more source

Chromosome Data and Karyotype Diversity of Anurans from Madagascar: Half a Century After the First Broad Cytosystematic Approach. [PDF]

Genes (Basel)
Mezzasalma M, Odierna G, Brunelli E, Guarino FM.   +3 more
europepmc   +1 more source

Seven new karyotypes for subfamily Cercosaurinae (Squamata, Gymnophthalmidae) with a synthesis of chromosomal data. [PDF]

Comp Cytogenet
Rachid LSF, Yonenaga-Yassuda Y, Rodrigues MT, Pellegrino KCM.   +3 more
europepmc   +1 more source

Case Report: Prenatal diagnosis of a rare complex fetal karyotype 47,U,t(10;13)(p15;q22)mat,+der(13)t(10;13)dmat resulting from 3:1 meiotic segregation of a maternal balanced translocation. [PDF]

Front Reprod Health
Deng GS, Zhang DH, Lai YQ, Song JJ, Pan JJ, Liang XF, Lu YH, Ning SS, Li WC, Li X, Chen YY, Li DR, Li LL, Liang YN.   +13 more
europepmc   +1 more source