August 23, 2011 - Connective Tissue Gene Tests (CTGT) today announced a number of new tests which provide clinicians with the most comprehensive testing for autosomal recessive osteogenesis imperfecta (OI) available.  CTGT now offers both DNA sequencing and Deletion / Duplication tests (HDT Array) for the following OI types and genes:

July 7, 2011 - Connective Tissue Gene Tests (CTGT) is pleased to announce the addition of 16 new tests for connective tissue disorders.

April 28, 2011 - Connective Tissue Gene Tests (CTGT) is pleased to announce new sequencing tests for 17 connective tissue disorders, and the addition of high density targeted array (HDT) deletion / duplication tests for an additional 8 disorders. 

December 22, 2010 — Connective Tissue Gene Tests (CTGT) continues to increase its repertoire of diagnostic tests, today announcing that it has added  new tests for Desbuquois dysplasia (DBQD; MIM 251450) and Torg-Winchester syndrome (MIM 259600).

August 18, 2010 — Connective Tissue Gene Tests (CTGT) continues to increase its repertoire of diagnostic tests, today announcing that it has added a new test for glomuvenous malformations (GVM; MIM 138000).

June 29, 2010 – Connective Tissue Gene Tests (CTGT) announced DNA sequencing testing for three additional disorders today, and simultaneously announced the availability of its proprietary High-Density Targeted Array testing methodology for an additional twenty-two (22) inherited connective tissue disorders.

June 1, 2010 — Connective Tissue Gene Tests (CTGT) announced today that it is now offering a proprietary High-Density Targeted Array for more than 50 inherited connective tissue disorders.  The new offering will provide physicians with an important new resource for diagnosing these disorders.

May 5, 2010 — Connective Tissue Gene Tests (CTGT) announced today that it is now offering molecular diagnostics for six additional disorders.

April 2, 2010 — Connective Tissue Gene Tests (CTGT) is pleased to announce the availability of molecular diagnostics for five additional inherited connective tissue disorders.

January 28, 2010 – As part of its on-going commitment to providing superlative service to its clients, Connective Tissue Gene Tests (CTGT) conducts an annual client survey.  The Company is pleased to report the results of its most recent survey.

January 18, 2010 — Connective Tissue Gene Tests (CTGT) announced today that it has added tests for two inherited disorders caused by mutations in the HSPG2 gene: Schwartz-Jampel syndrome, type 1 (SJS1; MIM 255800) and dyssegmental dysplasia, Silverman-Handmaker type (DDSH; MIM 224410). 

December 22, 2009 — Connective Tissue Gene Tests (CTGT) continues to increase its repertoire of diagnostic tests, today announcing that it has added a new test for Camurati-Engelmann disease (CED).

December 14, 2009 — Connective Tissue Gene Tests (CTGT) is pleased to announce the availability of molecular diagnostics for two additional inherited connective tissue disorders: Rickets, hypophosphatemic, autosomal recessive (ARHP) and Omodysplasia 1 (OMOD1).

November 9, 2009 — Connective Tissue Gene Tests (CTGT) is pleased to announce the availability of molecular diagnostics for eight additional disorders. This increases the company's repertoire for inherited connective tissue disorders to more than 90 tests.

October 8, 2009 - Experts from Connective Tissue Gene Tests (CTGT) were invited to appear on the TV program Tempo In Depth to discuss genetic testing and genetic counseling.  The program was aired today on Public Broadcasting Service affiliate WLVT, Allentown / Bethlehem / Easton, PA..

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