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American Journal of Medical Genetics. Part A
|
November 15, 2007
Raine syndrome: a rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findings
David Chitayat, Patrick Shannon, Sarah Keating, et al.
Pediatric Research
|
June 19, 2015
The ontogeny of P-glycoprotein in the developing human blood-brain barrier: implication for opioid toxicity in neonates
Jessica Lam, Stephanie Baello, Majid Iqbal, et al.
Journal of Genetic Counseling
|
April 20, 2011
Breast and ovarian cancer: the forgotten paternal contribution
Jeanna M McCuaig, Celia M T Greenwood, Cheryl Shuman, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC
|
September 2, 2017
No. 348-Joint SOGC-CCMG Guideline: Update on Prenatal Screening for Fetal Aneuploidy, Fetal Anomalies, and Adverse Pregnancy Outcomes
Francois Audibert, Isabelle De Bie, Jo-Ann Johnson, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC
|
September 2, 2017
François Audibert, Isabelle De Bie, Jo-Ann Johnson, et al.
Canadian Family Physician Medecin De Famille Canadien
|
September 18, 2007
Safety of codeine during breastfeeding: fatal morphine poisoning in the breastfed neonate of a mother prescribed codeine
Parvaz Madadi, Gideon Koren, James Cairns, et al.
Ultrasound Quarterly
|
September 7, 2007
The fetal cerebellar vermis: assessment for abnormal development by ultrasonography and magnetic resonance imaging
Ashley J Robinson, Susan Blaser, Ants Toi, et al.
American Journal of Medical Genetics. Part A
|
May 11, 2019
Alveolar capillary dysplasia with misalignment of the pulmonary veins and hypoplastic left heart sequence caused by an in frame deletion within FOXF1
Danielle K Bourque, Inara Chacon Fonseca, Andrea Staines, et al.
Eye (London, England)
|
February 26, 2022
Correction: Gene therapy: perspectives from young adults with Leber's congenital amaurosis
Melanie P Napier, Kavin Selvan, Robin Z Hayeems, et al.
The Journal of Allergy and Clinical Immunology
|
November 29, 2017
Dual loss of p110δ PI3-kinase and SKAP (KNSTRN) expression leads to combined immunodeficiency and multisystem syndromic features
Nigel Sharfe, Ariana Karanxha, Harjit Dadi, et al.
Page
of 36
Search research articles
Search
Showing results (161-170 of 353) with videos related to
Sort By:
Page
of 36
American Journal of Medical Genetics. Part A
|
November 15, 2007
Raine syndrome: a rare lethal osteosclerotic bone dysplasia. Prenatal diagnosis, autopsy, and neuropathological findings
David Chitayat, Patrick Shannon, Sarah Keating, et al.
Pediatric Research
|
June 19, 2015
The ontogeny of P-glycoprotein in the developing human blood-brain barrier: implication for opioid toxicity in neonates
Jessica Lam, Stephanie Baello, Majid Iqbal, et al.
Journal of Genetic Counseling
|
April 20, 2011
Breast and ovarian cancer: the forgotten paternal contribution
Jeanna M McCuaig, Celia M T Greenwood, Cheryl Shuman, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC
|
September 2, 2017
No. 348-Joint SOGC-CCMG Guideline: Update on Prenatal Screening for Fetal Aneuploidy, Fetal Anomalies, and Adverse Pregnancy Outcomes
Francois Audibert, Isabelle De Bie, Jo-Ann Johnson, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC
|
September 2, 2017
François Audibert, Isabelle De Bie, Jo-Ann Johnson, et al.
Canadian Family Physician Medecin De Famille Canadien
|
September 18, 2007
Safety of codeine during breastfeeding: fatal morphine poisoning in the breastfed neonate of a mother prescribed codeine
Parvaz Madadi, Gideon Koren, James Cairns, et al.
Ultrasound Quarterly
|
September 7, 2007
The fetal cerebellar vermis: assessment for abnormal development by ultrasonography and magnetic resonance imaging
Ashley J Robinson, Susan Blaser, Ants Toi, et al.
American Journal of Medical Genetics. Part A
|
May 11, 2019
Alveolar capillary dysplasia with misalignment of the pulmonary veins and hypoplastic left heart sequence caused by an in frame deletion within FOXF1
Danielle K Bourque, Inara Chacon Fonseca, Andrea Staines, et al.
Eye (London, England)
|
February 26, 2022
Correction: Gene therapy: perspectives from young adults with Leber's congenital amaurosis
Melanie P Napier, Kavin Selvan, Robin Z Hayeems, et al.
The Journal of Allergy and Clinical Immunology
|
November 29, 2017
Dual loss of p110δ PI3-kinase and SKAP (KNSTRN) expression leads to combined immunodeficiency and multisystem syndromic features
Nigel Sharfe, Ariana Karanxha, Harjit Dadi, et al.
Page
of 36