Search research articles
Contact Us
Filters
Showing results (1-10 of 20) with videos related to
Page
of 2
Sort By:
Current Opinion in Obstetrics & Gynecology
|
May 17, 2000
Genetic counselling in prenatally diagnosed non-chromosomal fetal abnormalities
D Chitayat, R Babul-Hirji
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 8, 2001
First-trimester increased nuchal translucency and fetal hypokinesia associated with Zellweger syndrome
J M Johnson, R Babul-Hirji, D Chitayat
Prenatal Diagnosis
|
March 4, 1998
Normal external genitalia in a female with classical congenital adrenal hyperplasia who was not treated during embryogenesis
N Quercia, D Chitayat, R Babul-Hirji, et al.
Journal of Genetic Counseling
|
August 12, 2015
Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling
R Z Hayeems, R Babul-Hirji, N Hoang, et al.
Journal of Genetic Counseling
|
November 16, 2013
Counseling and screening for cystic fibrosis in patients with congenital bilateral absence of the vas deferens: Patient perceptions
J L Fitzpatrick, E M Hutton, R Babul, et al.
American Journal of Medical Genetics
|
January 2, 1996
Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)]
D Chitayat, R Babul, M M Silver, et al.
American Journal of Human Genetics
|
January 1, 1995
Linkage analysis of the nail-patella syndrome
E Campeau, D Watkins, G A Rouleau, et al.
American Journal of Human Genetics
|
February 11, 1999
Brachydactyly type B: clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutation
Y Gong, D Chitayat, B Kerr, et al.
JAMA
|
November 17, 1993
Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease
R Babul, S Adam, B Kremer, et al.
American Journal of Medical Genetics
|
January 20, 1997
Limb defects in homozygous alpha-thalassemia: report of three cases
D Chitayat, M M Silver, K O'Brien, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Current Opinion in Obstetrics & Gynecology
|
May 17, 2000
Genetic counselling in prenatally diagnosed non-chromosomal fetal abnormalities
D Chitayat, R Babul-Hirji
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 8, 2001
First-trimester increased nuchal translucency and fetal hypokinesia associated with Zellweger syndrome
J M Johnson, R Babul-Hirji, D Chitayat
Prenatal Diagnosis
|
March 4, 1998
Normal external genitalia in a female with classical congenital adrenal hyperplasia who was not treated during embryogenesis
N Quercia, D Chitayat, R Babul-Hirji, et al.
Journal of Genetic Counseling
|
August 12, 2015
Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling
R Z Hayeems, R Babul-Hirji, N Hoang, et al.
Journal of Genetic Counseling
|
November 16, 2013
Counseling and screening for cystic fibrosis in patients with congenital bilateral absence of the vas deferens: Patient perceptions
J L Fitzpatrick, E M Hutton, R Babul, et al.
American Journal of Medical Genetics
|
January 2, 1996
Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)]
D Chitayat, R Babul, M M Silver, et al.
American Journal of Human Genetics
|
January 1, 1995
Linkage analysis of the nail-patella syndrome
E Campeau, D Watkins, G A Rouleau, et al.
American Journal of Human Genetics
|
February 11, 1999
Brachydactyly type B: clinical description, genetic mapping to chromosome 9q, and evidence for a shared ancestral mutation
Y Gong, D Chitayat, B Kerr, et al.
JAMA
|
November 17, 1993
Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease
R Babul, S Adam, B Kremer, et al.
American Journal of Medical Genetics
|
January 20, 1997
Limb defects in homozygous alpha-thalassemia: report of three cases
D Chitayat, M M Silver, K O'Brien, et al.
Page
of 2