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Clinical Genetics
|
March 1, 2005
A randomized trial comparing alternative approaches to prenatal diagnosis counseling in advanced maternal age patients
A G W Hunter, M Cappelli, L Humphreys, et al.
Pediatrics
|
May 1, 1990
Prenatal cocaine exposure and fetal vascular disruption
H 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 disorders
P 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 heterogeneity
N 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 22q11.2
N H Robin, G J Feldman, A L Aronson, et al.
Neurology
|
August 23, 2006
Autosomal dominant dystonia-plus with cerebral calcifications
Z K Wszolek, Y Baba, I R Mackenzie, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 47) with videos related to
Sort By:
Page
of 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 patients
A G W Hunter, M Cappelli, L Humphreys, et al.
Pediatrics
|
May 1, 1990
Prenatal cocaine exposure and fetal vascular disruption
H 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 disorders
P 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 heterogeneity
N 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 22q11.2
N H Robin, G J Feldman, A L Aronson, et al.
Neurology
|
August 23, 2006
Autosomal dominant dystonia-plus with cerebral calcifications
Z K Wszolek, Y Baba, I R Mackenzie, et al.
Page
of 5