Literature DB >> 4134631

An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.

P Jacobsen, M Hauge, K Henningsen, N Hobolth, M Mikkelsen, J Philip.   

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Year:  1973        PMID: 4134631     DOI: 10.1159/000152624

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


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  51 in total

1.  Nonrandom distribution of exchange points in patients with structural rearrangements.

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3.  Anticipation in familial leukemia.

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4.  Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation.

Authors:  C P Chen; F F Liu; S W Jan; C P Chen; C C Lan
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

5.  At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.

Authors:  D Smeets; C van Ravenswaaij; J de Pater; K Gerssen-Schoorl; J Van Hemel; G Janssen; A Smits
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

6.  The 11q-- syndrome: another case report.

Authors:  M T Mulcahy; J Jenkyn
Journal:  Hum Genet       Date:  1977-04-15       Impact factor: 4.132

7.  Fragile site long arm chromosome 16.

Authors:  K Sørensen; J Nielsen; V Holm; J Haahr
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

8.  Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome).

Authors:  C D Coldren; Z Lai; P Shragg; E Rossi; S C Glidewell; O Zuffardi; T Mattina; D D Ivy; L M Curfs; S N Mattson; E P Riley; M Treier; P D Grossfeld
Journal:  Neurogenetics       Date:  2008-10-15       Impact factor: 2.660

Review 9.  Inherited platelet dysfunction and hematopoietic transcription factor mutations.

Authors:  Natthapol Songdej; A Koneti Rao
Journal:  Platelets       Date:  2016-07-27       Impact factor: 3.862

10.  Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome).

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Journal:  Mol Cytogenet       Date:  2009-12-09       Impact factor: 2.009

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