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H Rehder

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Human Mutation|June 16, 2005

Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidneyR Wieser, B Fritz, R Ullmann, et al.

American Journal of Medical Genetics|April 6, 2000

Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissueA Aviram-Goldring, B Fritz, C Bartsch, et al.

Human Genetics|April 1, 1997

Microdeletion 22q11 in complex cardiovascular malformationsY Mehraein, C F Wippermann, I Michel-Behnke, et al.

Clinical Genetics|January 4, 2012

High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in TurkeyS Kalb, A O Caglayan, A Degerliyurt, et al.

Pageof 12

Search research articles

Showing results (111-120 of 114) with videos related to

Sort By:

Pageof 12

You have reached the last page of results.This site can display upto 114 results.

Human Mutation|June 16, 2005

Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidneyR Wieser, B Fritz, R Ullmann, et al.

American Journal of Medical Genetics|April 6, 2000

Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissueA Aviram-Goldring, B Fritz, C Bartsch, et al.

Human Genetics|April 1, 1997

Microdeletion 22q11 in complex cardiovascular malformationsY Mehraein, C F Wippermann, I Michel-Behnke, et al.

Clinical Genetics|January 4, 2012

High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in TurkeyS Kalb, A O Caglayan, A Degerliyurt, et al.

Pageof 12