Familial de Lange syndrome-Reference-Cited by-同舟云学术

Familial de Lange syndrome

Published:2008-04-23 Issue:3 Volume:2 Page:170-176
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Beratis Nicholas G.,Hsu Lillian Y. F.,Hirschhorn Kurt

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1971.tb00274.x/fullpdf

Reference25 articles.

1. De Lange Syndrome: Report of a case with an unusual karyotype;Berg;J med. Genet.,1967

2. Braehmann/de Lange syndrome;Bishun;Lancet,1965

3. Nanismo degenerativo tipo di Amsterdam (Typus amstelodamensis-malattia di Cornelia de Lange). Prezentazione di un caso e con-siderazioni di ordine genetico;Borghi;Acta Genet. meet. (Roma),1954

4. An inherited chromosome aberration in a girl with signs of de Lange syndrome;Broholm;Acta paediat. scand.,1968

5. Standardization in human cytogenetics;Chicago Conference;Birth Defects: Original Article Series,1966

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1. De Lange Syndrome;Atlas of Genetic Diagnosis and Counseling;2017

2. Gonadal mosaicism inARID1Bgene causes intellectual disability and dysmorphic features in three siblings;American Journal of Medical Genetics Part A;2015-09-23

3. De Lange Syndrome;Atlas of Genetic Diagnosis and Counseling;2015

4. Germline mosaicism in cornelia de lange syndrome: Dilemmas and risk figures;American Journal of Medical Genetics Part A;2013-05-21

5. Germline mosaicism in Cornelia de Lange syndrome;American Journal of Medical Genetics Part A;2012-05-11