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Development of high sensitivity potentiometric NOₓ sensor and its application to breath analysis

Sensors and actuators. B, Chemical, 2011-11, Vol.158 (1), p.292-298

2011

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Design, fabrication, and testing of MEMS-based miniaturized potentiometric nitric oxide sensors

Sensors and actuators. B, Chemical, 2014-12, Vol.204, p.183-189

2014

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A Prospective Study to Assess the Frequency of Familial Clustering of Congenital Bicuspid Aortic Valve

Journal of the American College of Cardiology, 1997-12, Vol.30 (7), p.1809-1812

1997

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Novel Carbon Dioxide Microsensor Based on Tin Oxide Nanomaterial Doped With Copper Oxide

IEEE sensors journal, 2009-03, Vol.9 (3), p.235-236

2009

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Gastroschisis: Clinical presentation and associations

American journal of medical genetics. Part C, Seminars in medical genetics, 2008-08, Vol.148C (3), p.219-230

2008

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Lathosterolosis: an inborn error of human and murine cholesterol synthesis due to lathosterol 5-desaturase deficiency

Human molecular genetics, 2003-07, Vol.12 (13), p.1631-1641

2003

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The external ear: More attention to detail may aid syndrome diagnosis and contribute answers to embryological questions

American journal of medical genetics. Part A, 2005-06, Vol.135A (3), p.237-250

2005

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Metal-oxide nanostructure and gas-sensing performance

Sensors and actuators. B, Chemical, 2009-04, Vol.138 (1), p.113-119

2009

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Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs

Canadian Medical Association journal, 2002-08, Vol.167 (4), p.367

Hunter, Alasdair G.W

2002

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Limb-body wall defect. Is there a defensible hypothesis and can it explain all the associated anomalies?

American journal of medical genetics. Part A, 2011-09, Vol.155A (9), p.2045-2059

2011

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Development of high sensitivity potentiometric NO x sensor and its application to breath analysis

Sensors and actuators. B, Chemical, 2011, Vol.158 (1), p.292-298

2011

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Learning the importance of double diagnosis

American journal of medical genetics. Part A, 2017-02, Vol.173 (2), p.568-568

Hunter, Alasdair G. W.

2017

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Considering the Embryopathogenesis of VACTERL Association

Molecular syndromology, 2013-02, Vol.4 (1-2), p.7-15

2013

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Oculocerebrocutaneous and encephalocraniocutaneous lipomatosis syndromes: Blind men and an elephant or separate syndromes?

American journal of medical genetics. Part A, 2006-04, Vol.140A (7), p.709-726

Hunter, Alasdair G.W.

2006

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Human equivalent of mouse disorganization: Has the case been made?

American journal of medical genetics. Part A, 2011-04, Vol.155A (4), p.792-804

Hunter, Alasdair G.W.

2011

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Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisis

Clinical genetics, 2009-04, Vol.75 (4), p.326-333

2009

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A randomized trial comparing alternative approaches to prenatal diagnosis counseling in advanced maternal age patients

Clinical genetics, 2005-04, Vol.67 (4), p.303-313

2005

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The intellectual disabilities evaluation and advice system (IDEAS): Outcome of the first 55 cases

American journal of medical genetics. Part A, 2014-05, Vol.164A (5), p.1102-1117

2014

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Absence of signs of systemic involvement in four patients with bilateral multiple facial angiofibromas

American journal of medical genetics. Part A, 2010-03, Vol.152A (3), p.657-664

2010

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Medical complications of achondroplasia: a multicentre patient review

Journal of medical genetics, 1998-09, Vol.35 (9), p.705-712

1998

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Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome

Journal of medical genetics, 2009-01, Vol.46 (1), p.9-13

2009

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Coffin-Lowry syndrome: A 20-year follow-up and review of long-term outcomes

American journal of medical genetics, 2002-09, Vol.111 (4), p.345-355

Hunter, Alasdair G.W.

2002

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Detailed assessment of the ear in Cornelia de Lange syndrome: Comparison with a control sample using the new dysmorphology guidelines

American journal of medical genetics. Part A, 2009-10, Vol.149A (10), p.2181-2192

2009

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Interstitial microdeletion of chromosome 1p in two siblings

American journal of medical genetics, 2002-08, Vol.111 (3), p.289-294

2002

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A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center

Clinical genetics, 2000-10, Vol.58 (4), p.299-308

2000

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Development of high sensitivity potentiometric NOₓ sensor and its application to breath analysis

Design, fabrication, and testing of MEMS-based miniaturized potentiometric nitric oxide sensors

A Prospective Study to Assess the Frequency of Familial Clustering of Congenital Bicuspid Aortic Valve

Novel Carbon Dioxide Microsensor Based on Tin Oxide Nanomaterial Doped With Copper Oxide

Gastroschisis: Clinical presentation and associations

Lathosterolosis: an inborn error of human and murine cholesterol synthesis due to lathosterol 5-desaturase deficiency

The external ear: More attention to detail may aid syndrome diagnosis and contribute answers to embryological questions

Metal-oxide nanostructure and gas-sensing performance

Medical genetics: 2. The diagnostic approach to the child with dysmorphic signs

Limb-body wall defect. Is there a defensible hypothesis and can it explain all the associated anomalies?

Development of high sensitivity potentiometric NO x sensor and its application to breath analysis

Learning the importance of double diagnosis

Considering the Embryopathogenesis of VACTERL Association

Oculocerebrocutaneous and encephalocraniocutaneous lipomatosis syndromes: Blind men and an elephant or separate syndromes?

Human equivalent of mouse disorganization: Has the case been made?

Escape of the yolk sac: a hypothesis to explain the embryogenesis of gastroschisis

A randomized trial comparing alternative approaches to prenatal diagnosis counseling in advanced maternal age patients

The intellectual disabilities evaluation and advice system (IDEAS): Outcome of the first 55 cases

Absence of signs of systemic involvement in four patients with bilateral multiple facial angiofibromas

Medical complications of achondroplasia: a multicentre patient review

Clinical experience in the evaluation of 30 patients with a prior diagnosis of FG syndrome

Coffin-Lowry syndrome: A 20-year follow-up and review of long-term outcomes

Detailed assessment of the ear in Cornelia de Lange syndrome: Comparison with a control sample using the new dysmorphology guidelines

Interstitial microdeletion of chromosome 1p in two siblings

A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center

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