H X Li|C P Chen - JoVE Visualize

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Human Genetics|February 1, 1992

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypesV Lindgren, C P Chen, C R Bryke, et al.

Genetic Counseling (Geneva, Switzerland)|April 23, 2005

A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephalyC P Chen, S R Chern, C J Lin, et al.

Genetic Counseling (Geneva, Switzerland)|May 23, 2012

Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndromeC P Chen, S P Lin, D S Lin, et al.

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

Direct transmission of the 18q- syndrome from mother to daughterC P Chen, S P Lin, S R Chern, et al.

Genetic Counseling (Geneva, Switzerland)|October 18, 2012

Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type IIIC P Chen, S P Lin, Y N Suo, et al.

The British Journal of Dermatology|April 16, 2013

Association between FOXP3 polymorphisms and vitiligo in a Han Chinese populationP Song, X-W Wang, H-X Li, et al.

Journal of Medical Genetics|October 10, 1997

Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephalyC P Chen, C C Lee, L F Chen, et al.

Anticancer Research|June 6, 1998

Detection of circulating cancer cells by nested reverse transcription-polymerase chain reaction of cytokeratin-19 (K19)--possible clinical significance in advanced gastric cancerK H Yeh, Y C Chen, S H Yeh, et al.

Pediatric Radiology|March 1, 1997

Skeletal deformities of acardius anceps: the gross and imaging featuresC P Chen, S L Shih, F F Liu, et al.

American Journal of Perinatology|May 1, 1996

Prenatal detection of the separation of the great toe, toe syndactyly, and large bilateral choroid plexus cysts in a fetus with trisomy 18C P Chen, F F Liu, S W Jan, et al.

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Showing results (281-290 of 398) with videos related to

Sort By:

Pageof 40

Human Genetics|February 1, 1992

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypesV Lindgren, C P Chen, C R Bryke, et al.

Genetic Counseling (Geneva, Switzerland)|April 23, 2005

A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephalyC P Chen, S R Chern, C J Lin, et al.

Genetic Counseling (Geneva, Switzerland)|May 23, 2012

Clinical imaging findings in a girl with Hutchinson-Gilford progeria syndromeC P Chen, S P Lin, D S Lin, et al.

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

Direct transmission of the 18q- syndrome from mother to daughterC P Chen, S P Lin, S R Chern, et al.

Genetic Counseling (Geneva, Switzerland)|October 18, 2012

Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type IIIC P Chen, S P Lin, Y N Suo, et al.

The British Journal of Dermatology|April 16, 2013

Association between FOXP3 polymorphisms and vitiligo in a Han Chinese populationP Song, X-W Wang, H-X Li, et al.

Journal of Medical Genetics|October 10, 1997

Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephalyC P Chen, C C Lee, L F Chen, et al.

Anticancer Research|June 6, 1998

Detection of circulating cancer cells by nested reverse transcription-polymerase chain reaction of cytokeratin-19 (K19)--possible clinical significance in advanced gastric cancerK H Yeh, Y C Chen, S H Yeh, et al.

Pediatric Radiology|March 1, 1997

Skeletal deformities of acardius anceps: the gross and imaging featuresC P Chen, S L Shih, F F Liu, et al.

American Journal of Perinatology|May 1, 1996

Prenatal detection of the separation of the great toe, toe syndactyly, and large bilateral choroid plexus cysts in a fetus with trisomy 18C P Chen, F F Liu, S W Jan, et al.

Pageof 40