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American Journal of Medical Genetics|September 20, 2001

Recurrent involvement of chromosomal region 6q21 in heterotaxyH Peeters, P Debeer, P Groenen, et al.

Clinical Genetics|April 1, 1994

Partial trisomy and monosomy 8p due to inversion duplicationJ J Engelen, C E de Die-Smulders, J P Fryns, et al.

American Journal of Medical Genetics. Part A|June 10, 2003

Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutationsPhilippe Debeer, H Peeters, S Driess, et al.

Genetic Counseling (Geneva, Switzerland)|November 6, 2002

Personality profiles of youngsters with velo-cardio-facial syndromeP Prinzie, A Swillen, A Vogels, et al.

Human Mutation|June 18, 2009

Deletions in the VPS13B (COH1) gene as a cause of Cohen syndromeI Balikova, A-E Lehesjoki, T J L de Ravel, et al.

International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|December 2, 2004

Immunohistochemical expression of CD10 antigen in uterine adenosarcomaF Amant, E Steenkiste, K Schurmans, et al.

Breast (Edinburgh, Scotland)|April 10, 2013

The prognostic role of preoperative and (early) postoperatively change in CA15.3 serum levels in a single hospital cohort of primary operable breast cancersO Brouckaert, A Laenen, H Wildiers, et al.

Journal of Medical Genetics|January 15, 2003

A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.

Human Mutation|December 8, 2004

DNMT3B mutations and DNA methylation defect define two types of ICF syndromeY L Jiang, M Rigolet, D Bourc'his, et al.

Human Genetics|February 28, 2003

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouseH Peeters, P Debeer, A Bairoch, et al.

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Showing results (811-820 of 883) with videos related to

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Pageof 89

American Journal of Medical Genetics|September 20, 2001

Recurrent involvement of chromosomal region 6q21 in heterotaxyH Peeters, P Debeer, P Groenen, et al.

Clinical Genetics|April 1, 1994

Partial trisomy and monosomy 8p due to inversion duplicationJ J Engelen, C E de Die-Smulders, J P Fryns, et al.

American Journal of Medical Genetics. Part A|June 10, 2003

Variable phenotype in Greig cephalopolysyndactyly syndrome: clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutationsPhilippe Debeer, H Peeters, S Driess, et al.

Genetic Counseling (Geneva, Switzerland)|November 6, 2002

Personality profiles of youngsters with velo-cardio-facial syndromeP Prinzie, A Swillen, A Vogels, et al.

Human Mutation|June 18, 2009

Deletions in the VPS13B (COH1) gene as a cause of Cohen syndromeI Balikova, A-E Lehesjoki, T J L de Ravel, et al.

International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|December 2, 2004

Immunohistochemical expression of CD10 antigen in uterine adenosarcomaF Amant, E Steenkiste, K Schurmans, et al.

Breast (Edinburgh, Scotland)|April 10, 2013

The prognostic role of preoperative and (early) postoperatively change in CA15.3 serum levels in a single hospital cohort of primary operable breast cancersO Brouckaert, A Laenen, H Wildiers, et al.

Journal of Medical Genetics|January 15, 2003

A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: proposal of a rapid enzymatic assay for screening mentally retarded patientsI Longo, S G M Frints, J-P Fryns, et al.

Human Mutation|December 8, 2004

DNMT3B mutations and DNA methylation defect define two types of ICF syndromeY L Jiang, M Rigolet, D Bourc'his, et al.

Human Genetics|February 28, 2003

PA26 is a candidate gene for heterotaxia in humans: identification of a novel PA26-related gene family in human and mouseH Peeters, P Debeer, A Bairoch, et al.

Pageof 89