Interstitial deletion of chromosome 22 in a patient with the DiGeorge malformation sequence
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Abstract
References (12)
High Resolution of Human Chromosomes
1976 • 786 citations
A deletion in chromosome 22 can cause digeorge syndrome
1981 • 366 citations
Contiguous gene syndromes: A component of recognizable syndromes
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Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.
1982 • 238 citations
The DiGeorge anomaly as a developmental field defect
1986 • 213 citations
The association of the DiGeorge anomalad with partial monosomy of chromosome 22
1982 • 191 citations
Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.
1988 • 183 citations
Di George syndrome and 22q11 rearrangements
1986 • 117 citations
Familial DiGeorge syndrome and associated partial monosomy of chromosome 22
1984 • 95 citations
Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).
1987 • 33 citations
Thymus deficiency in an infant with a chromosome t(18;22)(q12.2;p11.2)pat rearrangement
1986 • 27 citations
Issues and Reviews in Teratology
1987 • 2 citations