Literature DB >> 4126387

Monosomy of chromosome No. 22. A case report.

F DeCicco, M W Steele, S Pan, S C Park.   

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Year:  1973        PMID： 4126387     DOI： 10.1016/s0022-3476(73)80382-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  13 in total

1.  A male infant with monosomy 21.

Authors:  Y Kaneko; T Ikeuchi; M Sasaki; Y Stakae; S Kuwajima
Journal:  Humangenetik       Date:  1975-08-29

Review 2.  Defects in the determination of left-right asymmetry.

Authors:  M P Splitt; J Burn; J Goodship
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

3.  21 monosomy in a retarded female infant.

Authors:  K H Halloran; W R Breg; M J Mahoney
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

4.  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

Review 5.  The chromosomes of man--clinical and biologic significance. A review.

Authors:  J J Yunis; M E Chandler
Journal:  Am J Pathol       Date:  1977-08       Impact factor: 4.307

6.  Monosomy 22 with humoral immunodeficiency: is there an immunoglobulin chain deficit?

Authors:  J L García Miranda; A Otero Gómez; H Varela Ansedes; N Rancel Torres; C González Espinosa; C Cortabarría; G Sánchez Salgado
Journal:  J Med Genet       Date:  1983-02       Impact factor: 6.318

7.  Aortic root dilatation associated with partial trisomy 7(q31.2----qter).

Authors:  K B Roche; J W Moore; R B Surana; B E Wilson
Journal:  Pediatr Cardiol       Date:  1989       Impact factor: 1.655

8.  A deletion in chromosome 22 can cause DiGeorge syndrome.

Authors:  A de la Chapelle; R Herva; M Koivisto; P Aula
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 9.  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

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

Authors:  F Greenberg; F F Elder; P Haffner; H Northrup; D H Ledbetter
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025
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