Search research articles
Contact Us
Filters
Showing results (101-110 of 179) with videos related to
Page
of 18
Sort By:
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
October 6, 2011
Genetic-environmental interaction in a unique case of Muenke syndrome with intracranial hypertension
Nneamaka B Agochukwu, Benjamin D Solomon, Anna Zajaczkowska-Kielska, et al.
Orphanet Journal of Rare Diseases
|
July 16, 2025
Artificial intelligence for diagnosing rare bone diseases: a global survey of healthcare professionals
Behnam Javanmardi, Rebekah L Waikel, Tinatin Tkemaladze, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2010
Analysis of component findings in 79 patients diagnosed with VACTERL association
Benjamin D Solomon, Daniel E Pineda-Alvarez, Manu S Raam, et al.
American Journal of Medical Genetics. Part A
|
May 31, 2012
Patients within the Broad Holoprosencephaly Spectrum have Distinct and Subtle Ophthalmologic Anomalies: Response to Khan
Daniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Pediatric Dermatology
|
October 15, 2011
New syndrome of congenital circumferential skin folds associated with multiple congenital anomalies
Lina Basel-Vanagaite, Eli Sprecher, Andrea Gat, et al.
European Journal of Medical Genetics
|
February 15, 2011
Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association
Nneamaka B Agochukwu, Daniel E Pineda-Alvarez, Amelia A Keaton, et al.
American Journal of Medical Genetics. Part A
|
November 21, 2012
Clinical geneticists' views of VACTERL/VATER association
Benjamin D Solomon, Kelly A Bear, Virginia Kimonis, et al.
Cold Spring Harbor Molecular Case Studies
|
July 14, 2017
Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy
Dale L Bodian, Thierry Vilboux, Suchitra K Hourigan, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
December 18, 2013
Analysis of cardiac anomalies in VACTERL association
Bridget K Cunningham, Donald W Hadley, Hwaida Hannoush, et al.
American Journal of Medical Genetics. Part A
|
February 26, 2015
Expanding the phenotypic spectrum in EP300-related Rubinstein-Taybi syndrome
Benjamin D Solomon, Dale L Bodian, Alina Khromykh, et al.
Page
of 18
Search research articles
Search
Showing results (101-110 of 179) with videos related to
Sort By:
Page
of 18
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
October 6, 2011
Genetic-environmental interaction in a unique case of Muenke syndrome with intracranial hypertension
Nneamaka B Agochukwu, Benjamin D Solomon, Anna Zajaczkowska-Kielska, et al.
Orphanet Journal of Rare Diseases
|
July 16, 2025
Artificial intelligence for diagnosing rare bone diseases: a global survey of healthcare professionals
Behnam Javanmardi, Rebekah L Waikel, Tinatin Tkemaladze, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2010
Analysis of component findings in 79 patients diagnosed with VACTERL association
Benjamin D Solomon, Daniel E Pineda-Alvarez, Manu S Raam, et al.
American Journal of Medical Genetics. Part A
|
May 31, 2012
Patients within the Broad Holoprosencephaly Spectrum have Distinct and Subtle Ophthalmologic Anomalies: Response to Khan
Daniel E Pineda-Alvarez, Benjamin D Solomon, Erich Roessler, et al.
Pediatric Dermatology
|
October 15, 2011
New syndrome of congenital circumferential skin folds associated with multiple congenital anomalies
Lina Basel-Vanagaite, Eli Sprecher, Andrea Gat, et al.
European Journal of Medical Genetics
|
February 15, 2011
Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association
Nneamaka B Agochukwu, Daniel E Pineda-Alvarez, Amelia A Keaton, et al.
American Journal of Medical Genetics. Part A
|
November 21, 2012
Clinical geneticists' views of VACTERL/VATER association
Benjamin D Solomon, Kelly A Bear, Virginia Kimonis, et al.
Cold Spring Harbor Molecular Case Studies
|
July 14, 2017
Genomic analysis of an infant with intractable diarrhea and dilated cardiomyopathy
Dale L Bodian, Thierry Vilboux, Suchitra K Hourigan, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
December 18, 2013
Analysis of cardiac anomalies in VACTERL association
Bridget K Cunningham, Donald W Hadley, Hwaida Hannoush, et al.
American Journal of Medical Genetics. Part A
|
February 26, 2015
Expanding the phenotypic spectrum in EP300-related Rubinstein-Taybi syndrome
Benjamin D Solomon, Dale L Bodian, Alina Khromykh, et al.
Page
of 18