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Genome Research
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March 21, 1998
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb
S L Christian, N K Bhatt, S A Martin, et al.
Journal of Medical Genetics
|
October 26, 2010
Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability
Andres Moreno-De-Luca, Sandra L Helmers, Hui Mao, et al.
Prenatal Diagnosis
|
May 1, 1992
Risk factors associated with transcervical CVS losses
M S Golbus, J L Simpson, S E Fowler, et al.
The Journal of Clinical Investigation
|
June 1, 1988
Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa
D M Sosnoski, B S Emanuel, A L Hawkins, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2005
Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter
H L Archer, S Gupta, S Enoch, et al.
American Journal of Human Genetics
|
October 20, 2000
Partial paternal uniparental disomy of chromosome 6 in an infant with neonatal diabetes, macroglossia, and craniofacial abnormalities
S Das, C M Lese, M Song, et al.
Human Mutation
|
April 18, 2012
The introduction of arrays in prenatal diagnosis: a special challenge
Annalisa Vetro, Katelijne Bouman, Ros Hastings, et al.
The New England Journal of Medicine
|
August 27, 1992
A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group
L G Jackson, J M Zachary, S E Fowler, et al.
Genome Research
|
April 1, 1997
The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region
J S Sutcliffe, Y H Jiang, R J Galijaard, et al.
Genomics
|
June 1, 1996
A YAC contig of the human CC chemokine genes clustered on chromosome 17q11.2
K Naruse, M Ueno, T Satoh, et al.
Page
of 39
Search research articles
Search
Showing results (281-290 of 388) with videos related to
Sort By:
Page
of 39
Genome Research
|
March 21, 1998
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb
S L Christian, N K Bhatt, S A Martin, et al.
Journal of Medical Genetics
|
October 26, 2010
Adaptor protein complex-4 (AP-4) deficiency causes a novel autosomal recessive cerebral palsy syndrome with microcephaly and intellectual disability
Andres Moreno-De-Luca, Sandra L Helmers, Hui Mao, et al.
Prenatal Diagnosis
|
May 1, 1992
Risk factors associated with transcervical CVS losses
M S Golbus, J L Simpson, S E Fowler, et al.
The Journal of Clinical Investigation
|
June 1, 1988
Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa
D M Sosnoski, B S Emanuel, A L Hawkins, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2005
Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter
H L Archer, S Gupta, S Enoch, et al.
American Journal of Human Genetics
|
October 20, 2000
Partial paternal uniparental disomy of chromosome 6 in an infant with neonatal diabetes, macroglossia, and craniofacial abnormalities
S Das, C M Lese, M Song, et al.
Human Mutation
|
April 18, 2012
The introduction of arrays in prenatal diagnosis: a special challenge
Annalisa Vetro, Katelijne Bouman, Ros Hastings, et al.
The New England Journal of Medicine
|
August 27, 1992
A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group
L G Jackson, J M Zachary, S E Fowler, et al.
Genome Research
|
April 1, 1997
The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical region
J S Sutcliffe, Y H Jiang, R J Galijaard, et al.
Genomics
|
June 1, 1996
A YAC contig of the human CC chemokine genes clustered on chromosome 17q11.2
K Naruse, M Ueno, T Satoh, et al.
Page
of 39