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Angela E Lin

Showing results (111-120 of 170) with videos related to

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Hypertension (Dallas, Tex. : 1979)|May 13, 2009
Antihypertensive medication use during pregnancy and the risk of cardiovascular malformationsAlissa R Caton, Erin M Bell, Charlotte M Druschel, et al.
American Journal of Medical Genetics|September 5, 2002
Further delineation of cardiac abnormalities in Costello syndromeAngela E Lin, Paul D Grossfeld, Robert M Hamilton, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registrySiddharth K Prakash, Carolyn A Bondy, Cheryl L Maslen, et al.
Prenatal Diagnosis|April 22, 2009
Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardiaAngela E Lin, Barbara O'Brien, Laurie A Demmer, et al.
Journal of the American College of Cardiology|July 11, 2020
Characteristics of Adults With Congenital Heart Defects in the United StatesMichelle Gurvitz, Julie E Dunn, Ami Bhatt, et al.
Journal of Medical Genetics|September 24, 2018
Genome sequencing reveals a deep intronic splicing <i>ACVRL1</i> mutation hotspot in Hereditary Haemorrhagic TelangiectasiaWhitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell, et al.
Frontiers in Genetics|July 10, 2023
Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndromeAlexandra Garza Flores, Ida Nordgren, Maria Pettersson, et al.
American Journal of Medical Genetics. Part A|June 7, 2007
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndromeKaren W Gripp, Angela E Lin, Linda Nicholson, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 10, 2026
Psychotic Features in Myhre Syndrome: Evidence for Broader Neuropsychiatric SurveillanceMariz Ebuen, Vasudevan Krishnan, Kathleen Irby, et al.
American Journal of Medical Genetics. Part A|January 13, 2022
Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defectsGerarda Cappuccio, Nicola Brunetti-Pierri, Paul Clift, et al.
Pageof 17

Showing results (111-120 of 170) with videos related to

Sort By:
Pageof 17
Hypertension (Dallas, Tex. : 1979)|May 13, 2009
Antihypertensive medication use during pregnancy and the risk of cardiovascular malformationsAlissa R Caton, Erin M Bell, Charlotte M Druschel, et al.
American Journal of Medical Genetics|September 5, 2002
Further delineation of cardiac abnormalities in Costello syndromeAngela E Lin, Paul D Grossfeld, Robert M Hamilton, et al.
American Journal of Medical Genetics. Part A|September 9, 2016
Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registrySiddharth K Prakash, Carolyn A Bondy, Cheryl L Maslen, et al.
Prenatal Diagnosis|April 22, 2009
Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardiaAngela E Lin, Barbara O'Brien, Laurie A Demmer, et al.
Journal of the American College of Cardiology|July 11, 2020
Characteristics of Adults With Congenital Heart Defects in the United StatesMichelle Gurvitz, Julie E Dunn, Ami Bhatt, et al.
Journal of Medical Genetics|September 24, 2018
Genome sequencing reveals a deep intronic splicing <i>ACVRL1</i> mutation hotspot in Hereditary Haemorrhagic TelangiectasiaWhitney L Wooderchak-Donahue, Jamie McDonald, Andrew Farrell, et al.
Frontiers in Genetics|July 10, 2023
Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndromeAlexandra Garza Flores, Ida Nordgren, Maria Pettersson, et al.
American Journal of Medical Genetics. Part A|June 7, 2007
Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndromeKaren W Gripp, Angela E Lin, Linda Nicholson, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 10, 2026
Psychotic Features in Myhre Syndrome: Evidence for Broader Neuropsychiatric SurveillanceMariz Ebuen, Vasudevan Krishnan, Kathleen Irby, et al.
American Journal of Medical Genetics. Part A|January 13, 2022
Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defectsGerarda Cappuccio, Nicola Brunetti-Pierri, Paul Clift, et al.
Pageof 17