S R Chern - JoVE Visualize

Showing results (21-30 of 38) with videos related to

Pageof 4

Sort By:

Prenatal Diagnosis|March 10, 2001

Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasiaC P Chen, S R Chern, J C Shih, et al.

Genetic Counseling (Geneva, Switzerland)|January 22, 2005

De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delayC P Chen, S P Lin, S R Chern, et al.

Prenatal Diagnosis|April 5, 2001

Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial cleftsC P Chen, S R Chern, C Y Tzen, et al.

Genetic Counseling (Geneva, Switzerland)|February 7, 2012

Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disabilityC-P Chen, S-P Lin, S-R Chern, et al.

Genetic Counseling (Geneva, Switzerland)|February 26, 2013

Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delayC-P Chen, S-P Lin, Y-N Su, et al.

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

Pure distal 9p deletion in a female infant with cerebral palsyC-P Chen, S-P Lin, Y-N Su, et al.

Prenatal Diagnosis|June 1, 1997

Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive resultsC P Chen, S R Chern, F F Liu, et al.

The British Journal of Dermatology|February 1, 1997

Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascitesC P Chen, H C Chen, F F Liu, et al.

Genetic Counseling (Geneva, Switzerland)|October 28, 2011

A 24.2-Mb deletion of 4q12 --> q21.21 characterized by array CGH in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed pubertyC P Chen, S P Lin, Y N Su, 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.

Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:

Pageof 4

Prenatal Diagnosis|March 10, 2001

Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasiaC P Chen, S R Chern, J C Shih, et al.

Genetic Counseling (Geneva, Switzerland)|January 22, 2005

De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delayC P Chen, S P Lin, S R Chern, et al.

Prenatal Diagnosis|April 5, 2001

Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial cleftsC P Chen, S R Chern, C Y Tzen, et al.

Genetic Counseling (Geneva, Switzerland)|February 7, 2012

Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disabilityC-P Chen, S-P Lin, S-R Chern, et al.

Genetic Counseling (Geneva, Switzerland)|February 26, 2013

Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delayC-P Chen, S-P Lin, Y-N Su, et al.

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

Pure distal 9p deletion in a female infant with cerebral palsyC-P Chen, S-P Lin, Y-N Su, et al.

Prenatal Diagnosis|June 1, 1997

Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive resultsC P Chen, S R Chern, F F Liu, et al.

The British Journal of Dermatology|February 1, 1997

Cutis marmorata telangiectatica congenita associated with an elevated maternal serum human chorionic gonadotrophin level and transitory isolated fetal ascitesC P Chen, H C Chen, F F Liu, et al.

Genetic Counseling (Geneva, Switzerland)|October 28, 2011

A 24.2-Mb deletion of 4q12 --> q21.21 characterized by array CGH in a 131/2-year-old girl with short stature, mental retardation, developmental delay, hyperopia, exotropia, enamel defects, delayed tooth eruption and delayed pubertyC P Chen, S P Lin, Y N Su, 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.

Pageof 4