Genetic counseling (Geneva, Switzerland) - JoVE Visualize

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Genetic Counseling (Geneva, Switzerland)|January 1, 1994

Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defectP Petit, P Moerman, E Legius, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1990

Identification of carriers by screening for delta F508 deletion in a multi-generation cystic fibrosis familyM Claustres, M Desgeorges, P Kjellberg, et al.

Genetic Counseling (Geneva, Switzerland)|July 17, 1998

The Antley-Bixler syndrome. A new case without radiohumeral synostosisA Chabchoub, S Siala-Gaigi, Z Marrakchi, et al.

Genetic Counseling (Geneva, Switzerland)|July 17, 1998

Wiedemann-Rautenstrauch syndrome. A case report and review of the literatureC Stoll, F Labay, J Geisert, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?A Değerliyurt, G Ceylaner, H Koçak, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocationC-P Chen, S-P Lin, C-H Hsu, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocationZ Cetin, E Mihci, I Keser, et al.

Genetic Counseling (Geneva, Switzerland)|April 16, 2004

Alexithymia in Noonan syndromeW M Verhoeven, J L Hendrikx, M C MDoorakkers, et al.

Genetic Counseling (Geneva, Switzerland)|April 16, 2004

Neonatal detection of the 35delG mutation of the GJB2 gene in families at risk for deafnessC Bathelier, M François, G Lucotte

Genetic Counseling (Geneva, Switzerland)|August 6, 2005

Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic featuresM O Caliskan, S B Karauzum, E Mihci, et al.

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Showing results (671-680 of 1,155) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 1, 1994

Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defectP Petit, P Moerman, E Legius, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1990

Identification of carriers by screening for delta F508 deletion in a multi-generation cystic fibrosis familyM Claustres, M Desgeorges, P Kjellberg, et al.

Genetic Counseling (Geneva, Switzerland)|July 17, 1998

The Antley-Bixler syndrome. A new case without radiohumeral synostosisA Chabchoub, S Siala-Gaigi, Z Marrakchi, et al.

Genetic Counseling (Geneva, Switzerland)|July 17, 1998

Wiedemann-Rautenstrauch syndrome. A case report and review of the literatureC Stoll, F Labay, J Geisert, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

A new family with autosomal dominant porencephaly with a novel Col4A1 mutation. Are arachnoid cysts related to Col4A1 mutations?A Değerliyurt, G Ceylaner, H Koçak, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocationC-P Chen, S-P Lin, C-H Hsu, et al.

Genetic Counseling (Geneva, Switzerland)|August 11, 2012

Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocationZ Cetin, E Mihci, I Keser, et al.

Genetic Counseling (Geneva, Switzerland)|April 16, 2004

Alexithymia in Noonan syndromeW M Verhoeven, J L Hendrikx, M C MDoorakkers, et al.

Genetic Counseling (Geneva, Switzerland)|April 16, 2004

Neonatal detection of the 35delG mutation of the GJB2 gene in families at risk for deafnessC Bathelier, M François, G Lucotte

Genetic Counseling (Geneva, Switzerland)|August 6, 2005

Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic featuresM O Caliskan, S B Karauzum, E Mihci, et al.

Pageof 116