<--- Back to Details
First PageDocument Content
Genetic genealogy / Rare diseases / 17q21.31 microdeletion syndrome / 3q29 microdeletion syndrome / Alström syndrome / Down syndrome / Turner syndrome / Myelodysplastic syndrome / Chromosome 1 / Health / Syndromes / Genetics
Date: 2013-10-21 08:05:01
Genetic genealogy
Rare diseases
17q21.31 microdeletion syndrome
3q29 microdeletion syndrome
Alström syndrome
Down syndrome
Turner syndrome
Myelodysplastic syndrome
Chromosome 1
Health
Syndromes
Genetics

Marche des Maladies Rares – Alliance Maladies Rares Orphanet Report Series Rare Diseases collection December

Add to Reading List

Source URL: www.orpha.net

Download Document from Source Website

File Size: 1,20 MB

Share Document on Facebook

Similar Documents

Management of women with premature ovarian insufficiency SUMMARY Guideline of the European Society of Human Reproduction and Embryology

Management of women with premature ovarian insufficiency SUMMARY Guideline of the European Society of Human Reproduction and Embryology

DocID: 1psUi - View Document

Iowa Deafblind Registry New Referral You may SKIP all of pages 5 and 6 (columnsin the light grey font. Deafblind Project staff will include this information based on a review of the IEP.  Today’s Date:

Iowa Deafblind Registry New Referral You may SKIP all of pages 5 and 6 (columnsin the light grey font. Deafblind Project staff will include this information based on a review of the IEP. Today’s Date:

DocID: 1nMJp - View Document

Cerebral Cortex Advance Access published March 28, 2004  Brain Anatomy in Turner Syndrome: Evidence for Impaired Social and Spatial–Numerical Networks

Cerebral Cortex Advance Access published March 28, 2004 Brain Anatomy in Turner Syndrome: Evidence for Impaired Social and Spatial–Numerical Networks

DocID: 1eye0 - View Document

Noonan Syndrome First description The first description of Noonan syndrome (NS) dates back to 1883, when a student named Kobylinski reported on a male patient with several phenotypical characteristics. In 1963, paediatri

Noonan Syndrome First description The first description of Noonan syndrome (NS) dates back to 1883, when a student named Kobylinski reported on a male patient with several phenotypical characteristics. In 1963, paediatri

DocID: 1amYh - View Document

CHARGE Syndrome Foundation, Inc. 318 Half Day Road # 305 Buffalo Grove, IL7604 12th International Conference Schaumburg, IL — July 30 - August 2, 2015

CHARGE Syndrome Foundation, Inc. 318 Half Day Road # 305 Buffalo Grove, IL7604 12th International Conference Schaumburg, IL — July 30 - August 2, 2015

DocID: 1af9F - View Document