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Journal of Genetic Counseling
|
March 9, 2018
Informed Decision-Making in the Context of Prenatal Chromosomal Microarray
Jessica Baker, Cheryl Shuman, David Chitayat, et al.
American Journal of Medical Genetics. Part A
|
September 20, 2016
Rodriguez acrofacial dysostosis is caused by apparently de novo heterozygous mutations in the SF3B4 gene
Melita D Irving, Boyan I Dimitrov, Marja Wessels, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 15, 2011
Prospective validation of quantitative fluorescent polymerase chain reaction for rapid detection of common aneuploidies
Diane J Allingham-Hawkins, David Chitayat, Vincenzo Cirigliano, et al.
Molecular Medicine Reports
|
April 12, 2011
Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndrome
Manuela Morleo, Daniela Iaconis, David Chitayat, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2007
Fatal lung fibrosis associated with immunodeficiency and gonadal dysgenesis in 46XX sisters--a new syndrome
Raz Somech, Gino R Somers, David Chitayat, et al.
Prenatal Diagnosis
|
August 20, 2010
Fetal cardiac tumors: a single-center experience of 40 cases
Yoav Yinon, David Chitayat, Susan Blaser, et al.
Children (Basel, Switzerland)
|
August 26, 2023
Parental Preferences for Expanded Newborn Screening: What Are the Limits?
Nicole S Y Liang, Abby Watts-Dickens, David Chitayat, et al.
Human Mutation
|
August 9, 2005
SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders
Jürgen Kohlhase, David Chitayat, Dieter Kotzot, et al.
American Journal of Medical Genetics. Part A
|
July 26, 2017
Agenesis of the corpus callosum, developmental delay, autism spectrum disorder, facial dysmorphism, and posterior polymorphous corneal dystrophy associated with ZEB1 gene deletion
Ayeshah Chaudhry, Brian H Chung, Dimitri J Stavropoulos, et al.
American Journal of Medical Genetics. Part A
|
October 30, 2008
Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13)
Marzena Gajecka, Reem Saadeh, Katherine L Mackay, et al.
Page
of 36
Search research articles
Search
Showing results (121-130 of 353) with videos related to
Sort By:
Page
of 36
Journal of Genetic Counseling
|
March 9, 2018
Informed Decision-Making in the Context of Prenatal Chromosomal Microarray
Jessica Baker, Cheryl Shuman, David Chitayat, et al.
American Journal of Medical Genetics. Part A
|
September 20, 2016
Rodriguez acrofacial dysostosis is caused by apparently de novo heterozygous mutations in the SF3B4 gene
Melita D Irving, Boyan I Dimitrov, Marja Wessels, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 15, 2011
Prospective validation of quantitative fluorescent polymerase chain reaction for rapid detection of common aneuploidies
Diane J Allingham-Hawkins, David Chitayat, Vincenzo Cirigliano, et al.
Molecular Medicine Reports
|
April 12, 2011
Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndrome
Manuela Morleo, Daniela Iaconis, David Chitayat, et al.
American Journal of Medical Genetics. Part A
|
October 17, 2007
Fatal lung fibrosis associated with immunodeficiency and gonadal dysgenesis in 46XX sisters--a new syndrome
Raz Somech, Gino R Somers, David Chitayat, et al.
Prenatal Diagnosis
|
August 20, 2010
Fetal cardiac tumors: a single-center experience of 40 cases
Yoav Yinon, David Chitayat, Susan Blaser, et al.
Children (Basel, Switzerland)
|
August 26, 2023
Parental Preferences for Expanded Newborn Screening: What Are the Limits?
Nicole S Y Liang, Abby Watts-Dickens, David Chitayat, et al.
Human Mutation
|
August 9, 2005
SALL4 mutations in Okihiro syndrome (Duane-radial ray syndrome), acro-renal-ocular syndrome, and related disorders
Jürgen Kohlhase, David Chitayat, Dieter Kotzot, et al.
American Journal of Medical Genetics. Part A
|
July 26, 2017
Agenesis of the corpus callosum, developmental delay, autism spectrum disorder, facial dysmorphism, and posterior polymorphous corneal dystrophy associated with ZEB1 gene deletion
Ayeshah Chaudhry, Brian H Chung, Dimitri J Stavropoulos, et al.
American Journal of Medical Genetics. Part A
|
October 30, 2008
Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13)
Marzena Gajecka, Reem Saadeh, Katherine L Mackay, et al.
Page
of 36