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Journal Article
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2012, Volume 33, Issue 1, pp. 209.e3 - 209.e8
Journal Article
MOLECULAR CYTOGENETICS, ISSN 1755-8166, 05/2018, Volume 11
Background: A 46, XY sex reversal syndrome is characterized by discordant genetic and phenotypic sex, leading to normal external female genitalia, undeveloped... 
DMRT1 | Ring-chromosome-9 | Short-stature | Sex-reversal | RING | TESTIS | GENETICS & HEREDITY | SEX DETERMINATION | CHROMOSOMES | 46,XY-DSD | DELETION
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 09/2014, Volume 452, Issue 3, pp. 567 - 574
Journal Article
Journal Article
Leukemia, ISSN 0887-6924, 09/2013, Volume 27, Issue 9, pp. 1852 - 1860
Chronic myeloid malignancies are categorized to the three main categories myeloproliferative neoplasms (MPNs), myelodysplastic syndromes (MDSs) and MDS/MPN... 
monosomy 7 | MDS/MPN | SETBP1 | aCML | i(q10) | molecular marker | POLYCYTHEMIA-VERA | ACUTE MYELOID-LEUKEMIA | ESSENTIAL THROMBOCYTHEMIA | MOLECULAR MUTATIONS | ACTIVATING MUTATION | ONCOLOGY | CHRONIC MYELOPROLIFERATIVE DISORDERS | EXON 12 MUTATIONS | JAK2 | HEMATOLOGY | MYELODYSPLASTIC SYNDROMES | CHRONIC MYELOMONOCYTIC LEUKEMIA | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - diagnosis | Humans | Middle Aged | Male | Isochromosomes | Young Adult | Aged, 80 and over | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - genetics | Adult | Female | Nuclear Proteins - genetics | Chromosome Deletion | Proto-Oncogene Proteins c-cbl - genetics | Repressor Proteins - genetics | Mutation Rate | Myelodysplastic-Myeloproliferative Diseases - genetics | Chromosomes, Human, Pair 7 | Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative - mortality | Carrier Proteins - genetics | Myelodysplastic-Myeloproliferative Diseases - mortality | Myelodysplastic Syndromes - diagnosis | Myelodysplastic-Myeloproliferative Diseases - diagnosis | Bone Marrow - pathology | Myelodysplastic Syndromes - mortality | Aged | Myelodysplastic Syndromes - genetics | Mutation | Gene mutations | Physiological aspects | Genetic aspects | Research | Binding proteins | Myelodysplastic syndromes | Risk factors | Myeloproliferative disorders | Index Medicus
Journal Article
Taiwanese Journal of Obstetrics & Gynecology, ISSN 1028-4559, 08/2017, Volume 56, Issue 4, pp. 527 - 533
We present the association of paternal uniparental disomy (UPD) 9 with mosaicism for a small supernumerary marker chromosome 9 [sSMC(9)] and a supernumerary... 
9p duplication syndrome | Paternal uniparental disomy 9 | Supernumerary ring chromosome 9 | Small supernumerary marker chromosome 9 | VARIANTS | SEARCH | CHILD | OBSTETRICS & GYNECOLOGY | ORIGIN | SPECTRUM | DUPLICATION 9P | BANDS | MOLECULAR CYTOGENETIC CHARACTERIZATION
Journal Article