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J E Allanson

Showing results (41-50 of 47) with videos related to

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Clinical Genetics|March 1, 2005
A randomized trial comparing alternative approaches to prenatal diagnosis counseling in advanced maternal age patientsA G W Hunter, M Cappelli, L Humphreys, et al.
Pediatrics|May 1, 1990
Prenatal cocaine exposure and fetal vascular disruptionH E Hoyme, K L Jones, S D Dixon, et al.
Journal of Medical Genetics|November 1, 1991
Watson syndrome: is it a subtype of type 1 neurofibromatosis?J E Allanson, M Upadhyaya, G H Watson, et al.
Molecular Psychiatry|March 5, 2008
Face-brain asymmetry in autism spectrum disordersP Hammond, C Forster-Gibson, A E Chudley, et al.
Human Molecular Genetics|December 1, 1994
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneityN H Robin, G J Feldman, H F Mitchell, et al.
Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.
Neurology|August 23, 2006
Autosomal dominant dystonia-plus with cerebral calcificationsZ K Wszolek, Y Baba, I R Mackenzie, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Clinical Genetics|March 1, 2005
A randomized trial comparing alternative approaches to prenatal diagnosis counseling in advanced maternal age patientsA G W Hunter, M Cappelli, L Humphreys, et al.
Pediatrics|May 1, 1990
Prenatal cocaine exposure and fetal vascular disruptionH E Hoyme, K L Jones, S D Dixon, et al.
Journal of Medical Genetics|November 1, 1991
Watson syndrome: is it a subtype of type 1 neurofibromatosis?J E Allanson, M Upadhyaya, G H Watson, et al.
Molecular Psychiatry|March 5, 2008
Face-brain asymmetry in autism spectrum disordersP Hammond, C Forster-Gibson, A E Chudley, et al.
Human Molecular Genetics|December 1, 1994
Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneityN H Robin, G J Feldman, H F Mitchell, et al.
Nature Genetics|December 1, 1995
Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2N H Robin, G J Feldman, A L Aronson, et al.
Neurology|August 23, 2006
Autosomal dominant dystonia-plus with cerebral calcificationsZ K Wszolek, Y Baba, I R Mackenzie, et al.
Pageof 5