Literature DB >> 6502651

Parietal foramina in Saethre-Chotzen syndrome.

E M Thompson, M Baraitser, R D Hayward.   

Abstract

Mesh：

Year:  1984        PMID： 6502651      PMCID： PMC1049319          DOI： 10.1136/jmg.21.5.369

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


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  5 in total

1.  The Saethre-Chotzen syndrome.

Authors:  O A Pantke; M M Cohen; C J Witkop; M Feingold; B Schaumann; H C Pantke; R J Gorlin
Journal:  Birth Defects Orig Artic Ser       Date:  1975

2.  A concordant craniofacial dysostosis with enlarged parietal foramina in twins.

Authors:  H Z Lehrer; J W Familant
Journal:  Radiology       Date:  1969-01       Impact factor: 11.105

3.  Saethre-Chotzen syndrome: a broad and variable pattern of skeletal malformations.

Authors:  J M Friedman; J W Hanson; C B Graham; D W Smith
Journal:  J Pediatr       Date:  1977-12       Impact factor: 4.406

4.  Normal variants and congenital anomalies in the region of the obelion.

Authors:  G Currarino
Journal:  AJR Am J Roentgenol       Date:  1976-09       Impact factor: 3.959

5.  A family study of craniosynostosis, with probable recognition of a distinct syndrome.

Authors:  C O Carter; K Till; V Fraser; R Coffey
Journal:  J Med Genet       Date:  1982-08       Impact factor: 6.318
  5 in total
  9 in total

Review 1.  Enlarged parietal foramina: a rare forensic autopsy finding.

Authors:  Carlos Durão; Dina Carpinteiro; Frederico Pedrosa; Marcos P Machado; Eugénia Cunha
Journal:  Int J Legal Med       Date:  2015-08-02       Impact factor: 2.686

2.  Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Authors:  O Bartsch; W Wuyts; W Van Hul; J T Hecht; P Meinecke; D Hogue; W Werner; B Zabel; G K Hinkel; C M Powell; L G Shaffer; P J Willems
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

3.  The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500).

Authors:  W Wuyts; E Cleiren; T Homfray; A Rasore-Quartino; F Vanhoenacker; W Van Hul
Journal:  J Med Genet       Date:  2000-12       Impact factor: 6.318

Review 4.  Foramina parietalia permagna: familial and radiological evaluation of two cases and review of literature.

Authors:  Larissa Gabor; Huseyin Canaz; Gokhan Canaz; Nursu Kara; Elif Yilmaz Gulec; Ibrahim Alatas
Journal:  Childs Nerv Syst       Date:  2016-12-14       Impact factor: 1.475

5.  Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further families.

Authors:  A O Wilkie; S P Yang; D Summers; M D Poole; W Reardon; R M Winter
Journal:  J Med Genet       Date:  1995-03       Impact factor: 6.318

6.  Parietal foramina in the Saethre-Chotzen syndrome.

Authors:  I D Young; P G Swift
Journal:  J Med Genet       Date:  1985-10       Impact factor: 6.318

7.  Saethre-Chotzen syndrome: a clinical, EEG and neuroradiological study.

Authors:  M Elia; S A Musumeci; R Ferri; D Greco; C Romano; S Del Gracco; M C Stefanini
Journal:  Childs Nerv Syst       Date:  1996-11       Impact factor: 1.475

8.  Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis.

Authors:  Greg Holmes; Ana S Gonzalez-Reiche; Na Lu; Xianxiao Zhou; Joshua Rivera; Divya Kriti; Robert Sebra; Anthony A Williams; Michael J Donovan; S Steven Potter; Dalila Pinto; Bin Zhang; Harm van Bakel; Ethylin Wang Jabs
Journal:  Cell Rep       Date:  2020-07-07       Impact factor: 9.423

9.  An enlarged parietal foramen in the late archaic Xujiayao 11 neurocranium from Northern China, and rare anomalies among Pleistocene Homo.

Authors:  Xiu-Jie Wu; Song Xing; Erik Trinkaus
Journal:  PLoS One       Date:  2013-03-18       Impact factor: 3.240
  9 in total

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