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Showing results (61-70 of 79) with videos related to

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American Journal of Medical Genetics. Part A|April 8, 2015
Deletion of chromosome 8q22.1, a critical region for Nablus mask-like facial syndrome: four additional cases support a role of genetic modifiers in the manifestation of the phenotypeSaumya S Jamuar, Hatice Duzkale, Neslihan Duzkale, et al.
The Journal of Allergy and Clinical Immunology|October 18, 2011
Congenital malformations among infants born to women receiving montelukast, inhaled corticosteroids, and other asthma medicationsLinda M Nelsen, Kristine E Shields, Michael L Cunningham, et al.
Community Genetics|March 24, 2007
Knowledge of and attitudes about Alzheimer disease genetics: report of a pilot survey and two focus groupsT J Moscarillo, H Holt, M Perman, et al.
American Journal of Clinical Pathology|August 1, 1994
Toward objective quality assurance in cervical cytopathology. Correlation of cytopathologic diagnoses with detection of high-risk human papillomavirus typesM E Sherman, M H Schiffman, A T Lorincz, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 1, 1997
Evaluation of PAPNET testing as an ancillary tool to clarify the status of the "atypical" cervical smearM E Sherman, M H Schiffman, L J Mango, et al.
American Journal of Medical Genetics. Part A|October 15, 2015
Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizuresAlmundher Al-Maawali, Brenda J Barry, Anna Rajab, et al.
Acta Cytologica|February 28, 1998
ASCUS and AGUS criteria. International Academy of Cytology Task Force summary. Diagnostic Cytology Towards the 21st Century: An International Expert Conference and TutorialD Solomon, W J Frable, G P Vooijs, et al.
Neurology|October 1, 2013
Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humansL Benjamin Hills, Amira Masri, Kotaro Konno, et al.
American Journal of Human Genetics|April 14, 2015
Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and HypomyelinationTojo Nakayama, Almundher Al-Maawali, Malak El-Quessny, et al.
American Journal of Human Genetics|March 19, 2024
Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivationShreyas Bhat, Justine Rousseau, Coralie Michaud, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

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Pageof 8
American Journal of Medical Genetics. Part A|April 8, 2015
Deletion of chromosome 8q22.1, a critical region for Nablus mask-like facial syndrome: four additional cases support a role of genetic modifiers in the manifestation of the phenotypeSaumya S Jamuar, Hatice Duzkale, Neslihan Duzkale, et al.
The Journal of Allergy and Clinical Immunology|October 18, 2011
Congenital malformations among infants born to women receiving montelukast, inhaled corticosteroids, and other asthma medicationsLinda M Nelsen, Kristine E Shields, Michael L Cunningham, et al.
Community Genetics|March 24, 2007
Knowledge of and attitudes about Alzheimer disease genetics: report of a pilot survey and two focus groupsT J Moscarillo, H Holt, M Perman, et al.
American Journal of Clinical Pathology|August 1, 1994
Toward objective quality assurance in cervical cytopathology. Correlation of cytopathologic diagnoses with detection of high-risk human papillomavirus typesM E Sherman, M H Schiffman, A T Lorincz, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|June 1, 1997
Evaluation of PAPNET testing as an ancillary tool to clarify the status of the "atypical" cervical smearM E Sherman, M H Schiffman, L J Mango, et al.
American Journal of Medical Genetics. Part A|October 15, 2015
Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizuresAlmundher Al-Maawali, Brenda J Barry, Anna Rajab, et al.
Acta Cytologica|February 28, 1998
ASCUS and AGUS criteria. International Academy of Cytology Task Force summary. Diagnostic Cytology Towards the 21st Century: An International Expert Conference and TutorialD Solomon, W J Frable, G P Vooijs, et al.
Neurology|October 1, 2013
Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humansL Benjamin Hills, Amira Masri, Kotaro Konno, et al.
American Journal of Human Genetics|April 14, 2015
Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and HypomyelinationTojo Nakayama, Almundher Al-Maawali, Malak El-Quessny, et al.
American Journal of Human Genetics|March 19, 2024
Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivationShreyas Bhat, Justine Rousseau, Coralie Michaud, et al.
Pageof 8