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Clinical Genetics
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September 17, 2003
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality
H A Heilstedt, B C Ballif, L A Howard, et al.
Clinical Genetics
|
September 17, 2003
Huntington's disease: do future physicians and lawyers think eugenically?
B Elger, T Harding
Clinical Genetics
|
September 17, 2003
Split hand foot malformation is associated with a reduced level of Dactylin gene expression
D Basel, A DePaepe, M W Kilpatrick, et al.
Clinical Genetics
|
December 1, 1992
X-inactivation in girls with Rett syndrome
M H Kormann-Bortolotto, C G Woods, S H Green, et al.
Clinical Genetics
|
April 19, 2003
Landmarks in genetics through philately: Down syndrome
A E Chudley, B N Chodirker
Clinical Genetics
|
April 19, 2003
Genetic heterogeneity for a Nijmegen breakage-like syndrome
P Maraschio, E Spadoni, C Tanzarella, et al.
Clinical Genetics
|
April 19, 2003
Cerebro-oculo-facial-lymphatic syndrome
J M Milunsky, D M Capin
Clinical Genetics
|
April 19, 2003
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies
M C Digilio, A Angioni, M De Santis, et al.
Clinical Genetics
|
November 14, 2019
Chromatinopathies: A focus on Cornelia de Lange syndrome
Laura Avagliano, Ilaria Parenti, Paolo Grazioli, et al.
Clinical Genetics
|
June 1, 1988
Familial partial trisomy 5p resulting from segregation of an insertional translocation
K H Gustavson, P O Lundberg, P Nicol
Page
of 718
Search research articles
Search
Showing results (261-270 of 7,173) with videos related to
Sort By:
Page
of 718
Clinical Genetics
|
September 17, 2003
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality
H A Heilstedt, B C Ballif, L A Howard, et al.
Clinical Genetics
|
September 17, 2003
Huntington's disease: do future physicians and lawyers think eugenically?
B Elger, T Harding
Clinical Genetics
|
September 17, 2003
Split hand foot malformation is associated with a reduced level of Dactylin gene expression
D Basel, A DePaepe, M W Kilpatrick, et al.
Clinical Genetics
|
December 1, 1992
X-inactivation in girls with Rett syndrome
M H Kormann-Bortolotto, C G Woods, S H Green, et al.
Clinical Genetics
|
April 19, 2003
Landmarks in genetics through philately: Down syndrome
A E Chudley, B N Chodirker
Clinical Genetics
|
April 19, 2003
Genetic heterogeneity for a Nijmegen breakage-like syndrome
P Maraschio, E Spadoni, C Tanzarella, et al.
Clinical Genetics
|
April 19, 2003
Cerebro-oculo-facial-lymphatic syndrome
J M Milunsky, D M Capin
Clinical Genetics
|
April 19, 2003
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomalies
M C Digilio, A Angioni, M De Santis, et al.
Clinical Genetics
|
November 14, 2019
Chromatinopathies: A focus on Cornelia de Lange syndrome
Laura Avagliano, Ilaria Parenti, Paolo Grazioli, et al.
Clinical Genetics
|
June 1, 1988
Familial partial trisomy 5p resulting from segregation of an insertional translocation
K H Gustavson, P O Lundberg, P Nicol
Page
of 718