Literature DB >> 9508065

Molecular cytogenetic analysis of patients with holoprosencephaly and structural rearrangements of 7q.

G H Vance1, C Nickerson, L Sarnat, A Zhang, O Henegariu, N Morichon-Delvallez, M G Butler, C G Palmer.   

Abstract

The holoprosencephaly (HPE) sequence is a malformation complex with abnormal midline cleavage of the embryonic forebrain. HPE is genetically heterogeneous with at least 6 different chromosome regions containing genes involved in the expression of the phenotype. HPE3, recently identified as the human Sonic hedgehog gene, is localized to 7q36. We have used fluorescence in situ hybridization (FISH) and polymerase chain reaction (PCR) amplification in 5 cell lines from patients with HPE (3 cases), HPE and sacral agenesis (1 case), and microcephaly (1 case) to further define the structural rearrangements of the long arm of chromosome 7 in each case. All cell lines demonstrated loss of material in the critical region of HPE3 at band 7q36, which includes the Sonic hedgehog gene. We report here the analysis of these patient cell lines.

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Year:  1998        PMID: 9508065      PMCID: PMC6775641     

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  30 in total

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Journal:  Nature       Date:  1992-10-29       Impact factor: 49.962

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Authors:  W DEMYER; W ZEMAN; C G PALMER
Journal:  Pediatrics       Date:  1964-08       Impact factor: 7.124

3.  The 1993-94 Généthon human genetic linkage map.

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Journal:  Nat Genet       Date:  1994-06       Impact factor: 38.330

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Authors:  L C Tsui; H Donis-Keller; K H Grzeschik
Journal:  Cytogenet Cell Genet       Date:  1995

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Authors:  E D Green; J R Idol; R M Mohr-Tidwell; V V Braden; D C Peluso; R S Fulton; H F Massa; C L Magness; A M Wilson; J Kimura
Journal:  Hum Mol Genet       Date:  1994-03       Impact factor: 6.150

6.  Ectopic expression of Sonic hedgehog alters dorsal-ventral patterning of somites.

Authors:  R L Johnson; E Laufer; R D Riddle; C Tabin
Journal:  Cell       Date:  1994-12-30       Impact factor: 41.582

7.  Painting of human chromosomes with probes generated from hybrid cell lines by PCR with Alu and L1 primers.

Authors:  C Lengauer; H Riethman; T Cremer
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

8.  Physical mapping of the holoprosencephaly critical region on chromosome 7q36.

Authors:  F Gurrieri; B J Trask; G van den Engh; C M Krauss; A Schinzel; M J Pettenati; D Schindler; J Dietz-Band; G Vergnaud; S W Scherer
Journal:  Nat Genet       Date:  1993-03       Impact factor: 38.330

9.  Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

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Journal:  Nat Genet       Date:  1993-09       Impact factor: 38.330

10.  Duplication 3p21----3pter and cyclopia.

Authors:  D N Kurtzman; D L Van Dyke; C A Rich; L Weiss
Journal:  Am J Med Genet       Date:  1987-05
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  1 in total

1.  Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription.

Authors:  Giuseppe Di Stolfo; Maria Accadia; Sandra Mastroianno; Maria P Leone; Orazio Palumbo; Pietro Palumbo; Domenico Potenza; Pasquale Maccarone; Michele Sacco; Aldo Russo; Massimo Carella
Journal:  Mol Genet Genomic Med       Date:  2019-07-25       Impact factor: 2.183

  1 in total

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