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American Journal of Medical Genetics|September 5, 2002
Coffin-Lowry syndrome: a 20-year follow-up and review of long-term outcomesAlasdair G W HunterAmerican Journal of Medical Genetics. Part A|March 9, 2006
Oculocerebrocutaneous and encephalocraniocutaneous lipomatosis syndromes: blind men and an elephant or separate syndromes?Alasdair G W HunterAmerican Journal of Medical Genetics. Part A|March 19, 2011
Human equivalent of mouse disorganization: Has the case been made?Alasdair G W HunterCMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|August 29, 2002
Medical genetics: 2. The diagnostic approach to the child with dysmorphic signsAlasdair G W HunterAmerican Journal of Medical Genetics. Part A|February 22, 2005
Is multicenter collaborative research in clinical genetics dead and, if so, what killed it?Alasdair G W HunterAmerican Journal of Medical Genetics|September 20, 2002
Osteofibrous dysplasia: two affected male sibs and an unrelated girl with bilateral involvementAlasdair G W Hunter, James JarvisAmerican Journal of Medical Genetics. Part A|May 12, 2005
The external ear: more attention to detail may aid syndrome diagnosis and contribute answers to embryological questionsAlasdair G W Hunter, Takatoshi YotsuyanagiAmerican Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 26, 2008
Gastroschisis: clinical presentation and associationsAlasdair G W Hunter, Roger E StevensonAmerican Journal of Medical Genetics. Part A|April 23, 2003
A boy with developmental delay, malformations, and evidence of a connective tissue disorder: possibly a new type of cutis laxaLinlea Armstrong, Carmencita Jimenez, Alasdair G W HunterAmerican Journal of Medical Genetics. Part A|February 27, 2010
Absence of signs of systemic involvement in four patients with bilateral multiple facial angiofibromasAlasdair G W Hunter, Marjan M Nezarati, Lea VelsherPageof 2