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Literature DB >> 6712103

[Partial monosomy of the short arm of chromosome 10, associated with Rieger's syndrome and a Di George type partial immunodeficiency].

J Hervé, J F Warnet, E Jeaneau-Bellego, M F Portnoi, J L Taillemitte, F Hervé.

Abstract

Entities: Disease

Mesh：

Year: 1984 PMID： 6712103

Source DB: PubMed Journal: Ann Pediatr (Paris) ISSN： 0066-2097

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7 in total

1. A prospective cytogenetic study of 36 cases of DiGeorge syndrome.

Authors: D I Wilson; I E Cross; J A Goodship; J Brown; P J Scambler; H H Bain; J F Taylor; K Walsh; A Bankier; J Burn
Journal: Am J Hum Genet Date: 1992-11 Impact factor: 11.025

2. Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism.

Authors: M M Lai; P N Scriven; C Ball; A C Berry
Journal: J Med Genet Date: 1992-08 Impact factor: 6.318

3. A second locus for Rieger syndrome maps to chromosome 13q14.

Authors: J C Phillips; E A del Bono; J L Haines; A M Pralea; J S Cohen; L J Greff; J L Wiggs
Journal: Am J Hum Genet Date: 1996-09 Impact factor: 11.025

Review 4. Human chromosome 22.

Authors: J C Kaplan; A Aurias; C Julier; M Prieur; M F Szajnert
Journal: J Med Genet Date: 1987-02 Impact factor: 6.318

[Partial monosomy of the short arm of chromosome 10, associated with Rieger's syndrome and a Di George type partial immunodeficiency].

1. A prospective cytogenetic study of 36 cases of DiGeorge syndrome.

2. Simultaneous partial monosomy 10p and trisomy 5q in a case of hypoparathyroidism.

3. A second locus for Rieger syndrome maps to chromosome 13q14.

Review 4. Human chromosome 22.

5. Cytogenetic findings in a prospective series of patients with DiGeorge anomaly.

Review 6. Chromosome abnormalities and the genetics of congenital corneal opacification.

7. An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome.