Literature DB >> 7253002

Duplication-deletion with partial trisomy lq and partial monosomy 3p resulting from a maternal reciprocal translocation rcp (1;3) (q32;p25).

A Schinzel.   

Abstract

A mother with a translocation rcp (1;3) (q32;p25) gave birth to a son with duplication of 1q32 leads to qter and deletion of 3p25 leads to pter. At 17 1/2 years of age, the proband was severely mentally retarded and presented a pattern of multiple minor dysmorphic stigmata and anomalies, including hypertrichosis, synophrys, ocular hypertelorism, ptosis, convergent squint, cleft uvula nad narrow palate, poorly modelled auricles, funnel chest, kyphoscoliosis, umbilical and inguinal hernias, and cubitus valgus. He had normal stature and did not have any apparent malformations.

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Mesh:

Year:  1981        PMID: 7253002      PMCID: PMC1048662          DOI: 10.1136/jmg.18.1.64

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


  9 in total

1.  [Secondary trisomy 1 q due to a reciprocal maternal translocation].

Authors:  G Bourrouillou; P Colombies; P Blanc
Journal:  C R Seances Soc Biol Fil       Date:  1978

2.  Partial trisomy of the long arm of human chromosome 1 as demostrated by in situ hybridization with 5S ribosomal RNA.

Authors:  D M Steffensen; E H Chu; D P Speert; P M Wall; K Meilinger; R P Kelch
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

3.  Partial trisomy 1q due to tandem duplication.

Authors:  S Flatz; C Fonatsch
Journal:  Clin Genet       Date:  1979-06       Impact factor: 4.438

4.  Partial trisomy 1q syndrome.

Authors:  H Rehder; U Friedrich
Journal:  Clin Genet       Date:  1979-06       Impact factor: 4.438

5.  "De novo" trisomy 1q32 leads to 1qter and monosomy 3p25 leads to 3pter.

Authors:  E Yunis; H Egel; R Zúñiga; E Ramirez; O M Torres de Caballero; M Leibovici
Journal:  Hum Genet       Date:  1977-04-07       Impact factor: 4.132

6.  A patient with a partial deletion of the short arm of chromosome 3.

Authors:  M Verjaal; M B De Nef
Journal:  Am J Dis Child       Date:  1978-01

7.  Partial trisomy of the long arm of chromosome 1 due to a familial translocation t(1;10) (q32;q26).

Authors:  A Bonfante; M Stella; G Rossi
Journal:  Hum Genet       Date:  1978-12-29       Impact factor: 4.132

8.  Chromosome 3 duplication q/deletion p syndrome.

Authors:  R M Fineman; F Hecht; R C Ablow; R O Howard; W R Breg
Journal:  Pediatrics       Date:  1978-04       Impact factor: 7.124

9.  Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q--;6p+).

Authors:  K Taysi; G S Sekhon
Journal:  Hum Genet       Date:  1978-11-16       Impact factor: 4.132

  9 in total
  5 in total

1.  Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.

Authors:  H C Duba; M Erdel; J Löffler; L Bereuther; H Fischer; B Utermann; G Utermann
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  Three children with partial trisomy 1q and partial monosomy 3p.

Authors:  G T McCarthy; C N Fear; A C Berry
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

3.  Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.

Authors:  Anthony J Griswold; Deqiong Ma; Holly N Cukier; Laura D Nations; Mike A Schmidt; Ren-Hua Chung; James M Jaworski; Daria Salyakina; Ioanna Konidari; Patrice L Whitehead; Harry H Wright; Ruth K Abramson; Scott M Williams; Ramkumar Menon; Eden R Martin; Jonathan L Haines; John R Gilbert; Michael L Cuccaro; Margaret A Pericak-Vance
Journal:  Hum Mol Genet       Date:  2012-04-27       Impact factor: 6.150

4.  A girl with an interstitial deletion of the short arm of chromosome 3 studied with a high-resolution banding technique.

Authors:  Z Sichong; T H Bui; I Castro; L Iselius; S Håkansson; K M Lundmark
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes.

Authors:  Alicia Cervantes; Constanza García-Delgado; Fernando Fernández-Ramírez; Carolina Galaz-Montoya; Ariadna Berenice Morales-Jiménez; Karem Nieto-Martínez; Laura Gómez-Laguna; Judith Villa-Morales; Mónica Quintana-Palma; Jaime Berúmen; Susana Kofman; Verónica F Morán-Barroso
Journal:  BMC Med Genomics       Date:  2014-09-15       Impact factor: 3.063

  5 in total

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