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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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J A Goodship

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Clinical and Experimental Immunology|May 29, 2008

Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndromeA R Gennery, M A Slatter, J Rice, et al.

Nature Genetics|November 4, 2000

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defectsR N Bamford, E Roessler, R D Burdine, et al.

American Journal of Human Genetics|April 1, 2008

FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormalityJ A Fantes, E Boland, J Ramsay, et al.

Journal of Medical Genetics|November 14, 1997

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative studyA K Ryan, J A Goodship, D I Wilson, et al.

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Search research articles

Showing results (31-40 of 34) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 34 results.

Clinical and Experimental Immunology|May 29, 2008

Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndromeA R Gennery, M A Slatter, J Rice, et al.

Nature Genetics|November 4, 2000

Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defectsR N Bamford, E Roessler, R D Burdine, et al.

American Journal of Human Genetics|April 1, 2008

FISH mapping of de novo apparently balanced chromosome rearrangements identifies characteristics associated with phenotypic abnormalityJ A Fantes, E Boland, J Ramsay, et al.

Journal of Medical Genetics|November 14, 1997

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative studyA K Ryan, J A Goodship, D I Wilson, et al.

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