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         Shprintzen Syndrome:     more detail
  1. Syndrome Identification for Speech-Language Pathology: An Illustrated Pocketguide by Robert J. Shprintzen, 2000-01-15
  2. Syndrome Identification for Audiology: An Illustrated PocketGuide by Robert J. Shprintzen, 2001-02-02
  3. Velo-Cardio-Facial Syndrome, Volume I (Genetic Syndromes and Communication Disorders) by Robert J. Shprintzen, Karen J. Golding-Kushner, 2008-07-01
  4. Genetics, Syndromes and Communication Disorders by Robert J. Shprintzen, 1997-10-01
  5. Shprintzen-Goldberg craniosynostosis syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amy, MS, CGC Vance, 2005
  6. Growth Velocity, Weight Gain & Growth Charts for Velo-Cardio-Facial Syndrome: Management of Feeding and Swallowing Problems by Robert J. Shprintzen, 2010-01-01
  7. Velo-Cardio-Facial Syndrome Volume 2: Treatment of Communication Disorders by Karen J. Golding-Kushner, Robert J. Shprintzen, 2009-11-01
  8. Genetics, Syndromes and Communication Disorders by Robert J. Shprintzen,
  9. Velo-cardio-facial syndrome. (DVD included) (Genetic syndromes and communication by Robert J. and Karen J. Golding-Kushner. Shprintzen,

21. Shprintzen-Goldberg Syndrome GeneReviews NCBI Bookshelf
GoldbergShprintzen syndrome is a separate unrelated syndrome. Shprintzen-Goldberg syndrome has also been called craniosynostosis with arachnodactyly and abdominal hernias.
http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=sgs

22. DiGeorge Syndrome
Shprintzen named this group of features velocardio-facial syndrome, but the syndrome was also referred to as Shprintzen syndrome. In the 1980s, the technology was developed to
http://www.childrens.com/HealthLibrary/HealthLibContent.cfm?pageid=P01782

23. DiGeorge Syndrome
Shprintzen named this group of features velocardio-facial syndrome, but the syndrome was also referred to as Shprintzen syndrome. In the 1980s, the technology was developed to
http://www.chw.org/display/PPF/DocID/23047/router.asp

24. Foundation For Faces Of Children Pierre Robin Syndrome
The two most common are Stickler syndrome and velocardiofacial (or Shprintzen) syndrome, also known as VFCS. What is Stickler syndrome? Stickler syndrome is the basis for about 40
http://www.facesofchildren.org/Pierre Robin Syndrome

25. Shprintzen Syndrome - Definition Of Shprintzen Syndrome In The
2 deletion syndrome (22qDS) and includes phenotypes previously referred to as DiGeorge syndrome or Shprintzen syndrome.
http://medical-dictionary.thefreedictionary.com/Shprintzen syndrome

26. Personalized Light Blue Awareness Ribbon Pins For Addisons Disease
Prostate Cancer Scleroderma Shprintzen Syndrome Spay / Neuter Pets Thyroid Disease Trisomy 18 VeloCardio Facial Syndrome
http://www.personalizedcause.com/shop/collections/personalized/detail/p_lightblu

27. Velocardiofacial (Shprintzen) Syndrome An Important Syndrome For
We report the dysmorphological, genetic, and speech therapy aspects of 38 cases of velocardiofacial syndrome presenting to a craniofacial clinic and a specialised children's
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1015789/

28. 15 Known Cases Of Goldberg And Shprintzen Syndrome.no Answers.a
my 14 yr old daughter is one of 15 in the world with this syndrome.i lost my eldest daughter aged 4 12 yrs ago due to complications related to this syndrome. doctors and
http://www.medhelp.org/posts/Rare-Diseases/15-known-cases-of-goldberg-and-shprin

29. Shprintzen's Syndrome - Definition Of Shprintzen's Syndrome By The
Shprintzen syndrome Shprintzen's syndrome ShprintzenGoldberg Craniosynostosis Syndrome SHPRM SHPRP SHPS SHPSD SHPSU SHPT SHPT shpt. SHPTARBY SHPTV SHPU SHQ
http://www.thefreedictionary.com/Shprintzen's syndrome

30. Robert J. Shprintzen, Ph.D.
Widely published and recognized internationally, he is credited for delineating four genetic disorders, including velocardio-facial syndrome (also known as Shprintzen syndrome
http://www.pluralpublishing.com/author_Robert_Shprintzen.htm

31. Velo-Cardio-Facial Syndrome, Cincinnati Children's Hospital
Velocardiofacial Syndrome (or VCFS) is known by many names, including Shprintzen Syndrome, Craniofacial Syndrome, or Conotruncal Anomaly Face Syndrome.
http://www.cincinnatichildrens.org/health/heart-encyclopedia/disease/syndrome/vc

32. Shprintzen Syndrome Medical Definition
Medical definition for the term 'Shprintzen syndrome' Useful Websites. Medical Tourism Compare and save on surgery Global Translations
http://www.medilexicon.com/medicaldictionary.php?t=88195

33. Shprintzen Syndrome Definition Drugs.com
Definition of Shprintzen syndrome. Provided by Stedman's medical dictionary and Drugs.com. Includes medical terms and definitions.
http://www.drugs.com/dict/shprintzen-syndrome.html

34. The Genetics Of Shprintzen Syndrome - 22q11.2 Genetic Disorder
Shprintzen syndrome is a genetic disorder most commonly caused by a missing gene on chromosome 22, 22q11.2. It has a variety of symptoms including hypocalcaemia, cleft palate
http://www.brighthub.com/science/genetics/articles/71512.aspx

35. Goldberg-Shprintzen Syndrome - Humpath.com - Human Pathology
Definition GoldbergShprintzen syndrome associates microcephaly, mental retardation, Hirschsprung disease, bilateral generalized polymicogyria.
http://www.humpath.com/Goldberg-Shprintzen-syndrome

36. Shprintzen Syndrome - Wellsphere
Shprintzen Syndrome Free tips, articles, expert advice, videos, communities and more.
http://www.wellsphere.com/wellmix360/shprintzen-syndrome

37. Quinn Bradley Book Features VCFS Shprintzen Syndrome; Your Chance
2000 file phooto by Dick BlumeDr. Robert Shprintzen, who does research on Chromosome 22, with Karyotype Chromosome analysis on computer screen in the background at University
http://blog.syracuse.com/healthfitness/2009/04/quinn_bradley_book_features_vc.ht

38. The DRM WebWatcher Velo-Cardio-Facial Syndrome
It is also called Shprintzen syndrome, DiGeorge syndrome, craniofacial syndrome, conotruncal anomaly unusual face syndrome, 22q11, and catch 22.
http://www.disabilityresources.org/VELO.html

39. Shprintzen Syndrome - Rare Genetic Disease With
Shprintzen Syndrome rare genetic disease with heart defects and abnormal facial features. MEDgle is a medical and health search allowing you search your symptoms, diagnoses
http://www.medgle.com/rw/diagnoses/Shprintzen Syndrome

40. Omphalocele Gastroschisis Prune Belly
Abdominal Wall Defects omphalocele, gastroschisis fact sheet by IBIS
http://www.ibis-birthdefects.org/start/abdefect.htm

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