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American Journal of Medical Genetics. Part A
|
February 14, 2006
Discordant encephalocele in monozygotic twins
V de P Djientcheu, A Wonkam, A K Njamnshi, et al.
Human Molecular Genetics
|
January 1, 1994
Dinucleotide repeat polymorphism within ERCC5 gene
S Samec, S G Clarkson, J Blaschak, et al.
American Journal of Medical Genetics
|
April 14, 1997
Mitochondrial anomalies in a Swiss family with autosomal dominant myoglobinuria
R C Martin-Du Pan, M A Morris, H Favre, et al.
Receptors & Channels
|
November 25, 1998
Gene structure and chromosomal localization of the human P2X7 receptor
G N Buell, F Talabot, A Gos, et al.
Human Genetics
|
December 22, 1999
A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y
H Chen, C Rossier, M A Morris, et al.
Neurology
|
April 6, 2011
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE
I Bouchardy, O Steinlein, R Combi, et al.
Genomics
|
April 15, 1996
Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21
J L Blouin, G Duriaux-Sail, H Chen, et al.
Clinical Genetics
|
December 1, 1995
Trisomy 3 mosaicism on CVS: case report with literature review and propositions for investigation and counseling
C D Delozier-Blanchet, L Francipane, M A Morris, et al.
Receptors & Channels
|
January 1, 1995
Characterization and chromosomal localization of a human P2X receptor from the urinary bladder
S Valera, F Talabot, R J Evans, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
March 1, 1996
Estradiol conjugated to BSA releases oxytocin from synaptosome-containing homogenates from the medial preoptic area-hypothalamus
J D Caldwell, M A Morris, C H Walker, et al.
Page
of 16
Search research articles
Search
Showing results (101-110 of 152) with videos related to
Sort By:
Page
of 16
American Journal of Medical Genetics. Part A
|
February 14, 2006
Discordant encephalocele in monozygotic twins
V de P Djientcheu, A Wonkam, A K Njamnshi, et al.
Human Molecular Genetics
|
January 1, 1994
Dinucleotide repeat polymorphism within ERCC5 gene
S Samec, S G Clarkson, J Blaschak, et al.
American Journal of Medical Genetics
|
April 14, 1997
Mitochondrial anomalies in a Swiss family with autosomal dominant myoglobinuria
R C Martin-Du Pan, M A Morris, H Favre, et al.
Receptors & Channels
|
November 25, 1998
Gene structure and chromosomal localization of the human P2X7 receptor
G N Buell, F Talabot, A Gos, et al.
Human Genetics
|
December 22, 1999
A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y
H Chen, C Rossier, M A Morris, et al.
Neurology
|
April 6, 2011
Mutations of the orexin system, a regulator of sleep arousal, are not a common cause of ADNFLE
I Bouchardy, O Steinlein, R Combi, et al.
Genomics
|
April 15, 1996
Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21
J L Blouin, G Duriaux-Sail, H Chen, et al.
Clinical Genetics
|
December 1, 1995
Trisomy 3 mosaicism on CVS: case report with literature review and propositions for investigation and counseling
C D Delozier-Blanchet, L Francipane, M A Morris, et al.
Receptors & Channels
|
January 1, 1995
Characterization and chromosomal localization of a human P2X receptor from the urinary bladder
S Valera, F Talabot, R J Evans, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
March 1, 1996
Estradiol conjugated to BSA releases oxytocin from synaptosome-containing homogenates from the medial preoptic area-hypothalamus
J D Caldwell, M A Morris, C H Walker, et al.
Page
of 16