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Literature DB >> 3236358

Long arm deletion of chromosome 22.

G Kirshenbaum¹, M Chmura, D P Rhone.

Abstract

Mesh：

Year: 1988 PMID： 3236358 PMCID： PMC1051586 DOI： 10.1136/jmg.25.11.780

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

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3 in total

1. [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].

Authors: J LEJEUNE; R BERGER; M O RETHORE; L ARCHAMBAULT; H JEROME; S THIEFFRY; J AICARDI; M BROYER; J LAFOURCADE; J CRUVEILLER; R TURPIN
Journal: C R Hebd Seances Acad Sci Date: 1964-11-30

2. Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.

Authors: R J Warren; D L Rimoin; R L Summitt
Journal: Am J Hum Genet Date: 1973-01 Impact factor: 11.025

3. Clinical and cytogenetic studies of two infants with partial monosomy G.

Authors: T Maeda; M Ohno; H Nishida
Journal: Hum Genet Date: 1977-03-14 Impact factor: 4.132

3 in total

7 in total

1. Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter).

Authors: D R Romain; J Goldsmith; H Cairney; L M Columbano-Green; R H Smythe; R G Parfitt
Journal: J Med Genet Date: 1990-09 Impact factor: 6.318

2. Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.

Authors: Roberto Mendoza-Londono; Edward Lammer; Rosemarie Watson; John Harper; Atsushi Hatamochi; Saori Hatamochi-Hayashi; Dobrawa Napierala; Pia Hermanns; Sinead Collins; Benjamin B Roa; Madhuri R Hedge; Keiko Wakui; Diep Nguyen; David W Stockton; Brendan Lee
Journal: Am J Hum Genet Date: 2005-05-27 Impact factor: 11.025

Long arm deletion of chromosome 22.

1. [PARTIAL MONOSOMY FOR A SMALL ACROCENTRIC CHROMOSOME].

2. Identification by fluorescent microscopy of the abnormal chromosomes associated with the G-deletion syndromes.

3. Clinical and cytogenetic studies of two infants with partial monosomy G.

1. Partial monosomy for chromosome 22 in a patient with del(22)(pter----q13.1::q13.33----qter).

2. Characterization of a new syndrome that associates craniosynostosis, delayed fontanel closure, parietal foramina, imperforate anus, and skin eruption: CDAGS.

3. The phenotypic effects of chromosome rearrangement involving bands 7q21.3 and 22q13.3.

4. The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome).

5. Phenotypic correlations in a patient with ring chromosome 22.

6. Clinical, cytogenetic, and molecular characterization of seven patients with deletions of chromosome 22q13.3.

7. Ring chromosome 22: a review of the literature and first report from India.