Literature DB >> 1126048

Physical and mental defect of chromosomal origin in four individuals of the same family. Trisomy for the short arm of 9.

C E Blank, D C Colver, A M Potter, J McHugh, J Lorber.   

Abstract

A family with the reciprocal translocation t(9;22)(q13;q11) segregating in genetically balanced and unbalanced form is identified. The clinical features of four members with trisomy for the short arm of 9, and the proximal part of the long arm of 9, are described in detail. Features in common are summarized and compared with developmental abnormality observed in other examples of trisomy for the short arm of 9. An attempt is made to delineate further the clinical features commonly seen in trisomy for the short arm of 9.

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Year:  1975        PMID: 1126048     DOI: 10.1111/j.1399-0004.1975.tb00328.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  14 in total

1.  Possible intrachromosomal duplication in a case of trisomy 9p.

Authors:  H Chiyo; J Furuyama; N Suehara; Y Obashi; H Kikkawa
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

2.  Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Authors:  A Schinzel; K Hayashi; W Schmid
Journal:  Humangenetik       Date:  1975-12-23

3.  De novo trisomy 9pter leads to q13.

Authors:  N B Kardon; H R Salwen; M A Krauss; J G Davis; E C Jenkins
Journal:  Hum Genet       Date:  1977-06-30       Impact factor: 4.132

4.  Familial trisomy 9p and spinal muscular atrophy: clinical, cytogenetic and embryological findings.

Authors:  M Tolksdorf; J Kunze; G Gross-Selbeck; K Sperling; R D Wegner; V Wieczorek; M Vogel
Journal:  Eur J Pediatr       Date:  1977-08-23       Impact factor: 3.183

5.  Complex translocation t(9;21)(9;22)(q12p13)(q12q11) in the family of a child with 9p trisomy syndrome.

Authors:  B Dallapiccola; G Bollea; C Mazzilli; E Gandini
Journal:  Hum Genet       Date:  1976-07-07       Impact factor: 4.132

Review 6.  Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

Authors:  P Jalbert; B Sele
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

Review 7.  Viability thresholds for partial trisomies and monosomies. A study of 1,159 viable unbalanced reciprocal translocations.

Authors:  O Cohen; C Cans; M A Mermet; J Demongeot; P Jalbert
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132

8.  Radiological abnormalities associated with anomalies of the ninth chromosome.

Authors:  D W Pilling; R K Levick
Journal:  Pediatr Radiol       Date:  1978-02-28

9.  t(9/22) with centric fission and NOR translocation leading to a case of pure 9p trisomy in the offspring.

Authors:  N Archidiacono; M Rocchi; U de Vonderweid; G Filippi
Journal:  Hum Genet       Date:  1978-02-16       Impact factor: 4.132

10.  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

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