Results 161 to 170 of about 13,528 (181)

A Two-Country Questionnaire Study of Biomedical Student Opinions Regarding Online Teaching During COVID-19. [PDF]

open access: yesEpidemiologia (Basel)
Ognjanovic I   +10 more
europepmc   +1 more source

Interstitial 1q43-q43 deletion with left ventricular noncompaction myocardium

European Journal of Medical Genetics, 2006
We describe a newborn infant with del(1)(q) syndrome, presenting with rare congenital cardiomyopathy and left ventricular noncompaction myocardium (LVNC), as well as typical clinical features such as facial dysmorphism and psychomotor retardation. Although conventional chromosome banding at 850 bands per haploid set indicated a karyotype of 46,XX,add(1)
Nobuko, Kanemoto   +7 more
openaire   +2 more sources

Interstitial deletion of 1q42.13-q43 with Duane retraction syndrome

Journal of American Association for Pediatric Ophthalmology and Strabismus, 2007
Duane retraction syndrome is a congenital eye movement disorder characterized by failure of the sixth cranial nerve or nucleus to develop properly, resulting in restriction of abduction, narrowing of the palpebral fissure, and retraction of the globe on attempted adduction and/or restricted adduction. The gene loci of Duane syndrome have been mapped on
Zenichiro, Kato   +2 more
openaire   +2 more sources

MPEC 2023-Q43 : 2023 QA1

2023
The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
openaire   +1 more source

Molecular cytogenetic characterization of a t(1;5)(q43;q33) in a mesenchymal chondrosarcoma

Cancer Genetics and Cytogenetics, 2010
1. Section for Cancer Cytogenetics, Institute for Medical Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway 2. Department of Oncology, Division of Cancer Medicine and Radiotherapy, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway 3.
Kaja Beate Nyquist   +6 more
openaire   +1 more source

A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter→q23∼24::q23∼24→q43→neo→q43→qter) and tetrasomy of chromosomes 8 and 21

Cancer Genetics and Cytogenetics, 2009
Abstract Hyperdiploidy is rarely observed in childhood acute myeloid leukemia (AML). Described here is the case of a 2½-year-old girl with AML-M5 and 51 chromosomes characterized by double tetrasomy of chromosomes 8 and 21 and also a neocentric derivative chromosome neo(1)(qter→q23∼24::q23∼24→q43→neo→q43→qter).
Amanda Faria de Figueiredo   +8 more
openaire   +1 more source

Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21 → q25) and del(1)(q41 → q43)

Clinical Genetics, 1985
Two unrelated children, one with a proximal interstitial deletion 1 (l(pter → q21: :q25 → qter)) and the other one with a distal interstitial deletion 1 (l(pter → q41: :q43 → qter)) are presented. The clinical features of the patient with a proximal deletion (q21‐q25) correspond with those of eight earlier reported cases with a deletion lq21/22/23 ...
F A, Beemer   +3 more
openaire   +2 more sources

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