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E F Percin

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Genetic Counseling (Geneva, Switzerland)|September 15, 2006

A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluationsM Yirmibes Karaoguz, A Biri, E Pala, et al.

Nature Genetics|August 10, 2000

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.

Clinical Genetics|March 13, 2016

Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosisS Boppudi, N Bögershausen, H B Hove, et al.

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Search research articles

Showing results (11-20 of 13) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 13 results.

Genetic Counseling (Geneva, Switzerland)|September 15, 2006

A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluationsM Yirmibes Karaoguz, A Biri, E Pala, et al.

Nature Genetics|August 10, 2000

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.

Clinical Genetics|March 13, 2016

Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosisS Boppudi, N Bögershausen, H B Hove, et al.

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