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Case report of 5 siblings: malnutrition? Rickets? DiGeorge syndrome? Developmental delay?Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndromeReview of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplantsThe fundamental contribution of Robert A. Good to the discovery of the crucial role of thymus in mammalian immunityThe T-box factor MLS-1 acts as a molecular switch during specification of nonstriated muscle in C. elegansDecreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn miceAgenesis of the corpus callosum associated with DiGeorge-velocardiofacial syndrome: a case report and review of the literature.Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome.The dynamics of T-cell receptor repertoire diversity following thymus transplantation for DiGeorge anomalyA new recessive syndrome of unusual facies and multiple structural abnormalities.Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.Increased prevalence of immunoglobulin A deficiency in patients with the chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).Anal anomalies: an uncommon feature of velocardiofacial (Shprintzen) syndrome?Prenatal diagnosis by FISH of a 22q11 deletion in two familiesInterrupted right aortic arch in DiGeorge syndrome.Clinical course and outcome predictors of critically ill infants with complete DiGeorge anomaly following thymus transplantationMechanisms of tolerance to parental parathyroid tissue when combined with human allogeneic thymus transplantation.Endocrine aspects of the 22q11.2 deletion syndrome.Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome.Hypoparathyroidism and 22q11 deletion syndromeA prospective cytogenetic study of 36 cases of DiGeorge syndromeCytogenetic findings in a prospective series of patients with DiGeorge anomalyShort stature, mental retardation, and hypoparathyroidism: a new syndrome.A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic featuresQualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia.The teratogenic effects of a bis(dichloroacetyl)diamine on hamster embryos. Aortic arch anomalies and the pathogenesis of the DiGeorge syndrome.Molecular characterization of the marker chromosome associated with cat eye syndromePrediction, prevention and personalisation of medication for the prenatal period: genetic prenatal tests for both rare and common diseasesReal-time magnetic resonance imaging aids prenatal diagnosis of isolated cleft palate.Human T cell reconstitution in DiGeorge syndrome and HIV-1 infection.Erythroderma/generalized exfoliative dermatitis in pediatric practice: an overview.Microgyria in the distribution of the middle cerebral artery in a patient with DiGeorge syndrome.Factors affecting success of thymus transplantation for complete DiGeorge anomalyLong-term tolerance to allogeneic thymus transplants in complete DiGeorge anomalyThymus transplantation in complete DiGeorge anomaly.Parathyroid hormone reserve in 22q11.2 deletion syndrome.Thymus transplantation.Head and neck manifestations of 22q11.2 deletion syndromes.
P2860
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P2860
description
1979 nî lūn-bûn
@nan
1979年の論文
@ja
1979年論文
@yue
1979年論文
@zh-hant
1979年論文
@zh-hk
1979年論文
@zh-mo
1979年論文
@zh-tw
1979年论文
@wuu
1979年论文
@zh
1979年论文
@zh-cn
name
The spectrum of the DiGeorge syndrome.
@en
type
label
The spectrum of the DiGeorge syndrome.
@en
prefLabel
The spectrum of the DiGeorge syndrome.
@en
P2093
P1476
The spectrum of the DiGeorge syndrome.
@en
P2093
Beckwith JB
Tenckhoff L
P304
P356
10.1016/S0022-3476(79)80207-3
P407
P577
1979-06-01T00:00:00Z