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Point Mutations in Human GLI3 Cause Greig Syndrome

Human molecular genetics, 1997-10, Vol.6 (11), p.1979-1984

1997

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Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations

American journal of medical genetics, 2003-07, Vol.120A (1), p.49-58

2003

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Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome

Human molecular genetics, 1999-09, Vol.8 (9), p.1769-1777

1999

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Gene symbol: GLI3. Disease: Pallister-Hall syndrome

Human genetics, 2004-03, Vol.114 (4), p.403-403

2004

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Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality

Clinical genetics, 1997-12, Vol.52 (6), p.436-441

1997

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Lutealphasensubstitution in der ART – vaginale Progesteronsubstitution versus subkutane Applikation in der täglich klinischen Anwendung

Geburtshilfe und Frauenheilkunde, 2018, Vol.78 (10)

2018

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All known human H1 histone genes except the H1(0) gene are clustered on chromosome 6

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.649-654

1993

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All Human Genes of the Uteroglobin Family Are Localized on Chromosome 11q12.2 and Form a Dense Cluster

Annals of the New York Academy of Sciences, 2000-12, Vol.923 (1), p.25-42

2000

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Molecular Characterization of Human Zyxin

The Journal of biological chemistry, 1996-12, Vol.271 (49), p.31470-31478

1996

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Influence of different oxygen concentrations on mouse embryo development using time-lapse-imaging

Geburtshilfe und Frauenheilkunde, 2018, Vol.78 (10)

2018

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Effects of opening the incubator on morphokinetics in mouse embryos

Geburtshilfe und Frauenheilkunde, 2018, Vol.78 (10)

2018

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Human Sp4 transcription factor gene (SP4) maps to chromosome 7p15

Genomics (San Diego, Calif.), 1995-04, Vol.26 (3), p.631-633

1995

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Regional Localization of 725 Human Chromosome 7-Specific Yeast Artificial Chromosome Clones

Genomics (San Diego, Calif.), 1994-07, Vol.22 (2), p.439-448

1994

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The human S3a ribosomal protein: sequence, location and cell-free transcription of the functional gene

Gene, 1996-03, Vol.169 (2), p.179-185

1996

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Human Sp3 Transcriptional Regulator Gene (SP3) Maps to Chromosome 2q31

Genomics (San Diego, Calif.), 1996-11, Vol.37 (3), p.410-412

1996

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Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: Not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individual

American journal of medical genetics, 2000-01, Vol.90 (3), p.239-242

2000

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All known human H1 histone genes except the H10 gene are clustered on chromosome 6

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.649-654

1993

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Gene symbol: GLI3. Disease: Pallister-Hall syndrome

Human genetics, 2003-01, Vol.112 (1), p.103-103

2003

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Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndrome

Human genetics, 2003-01, Vol.112 (1), p.103-103

2003

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Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality

Clinical Genetics, 1997, Vol.52 (6), p.436-441

1997

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Point Mutations in Human GLI3 Cause Greig Syndrome

Variable phenotype in Greig cephalopolysyndactyly syndrome: Clinical and radiological findings in 4 independent families and 3 sporadic cases with identified GLI3 mutations

Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome

Gene symbol: GLI3. Disease: Pallister-Hall syndrome

Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality

Lutealphasensubstitution in der ART – vaginale Progesteronsubstitution versus subkutane Applikation in der täglich klinischen Anwendung

All known human H1 histone genes except the H1(0) gene are clustered on chromosome 6

All Human Genes of the Uteroglobin Family Are Localized on Chromosome 11q12.2 and Form a Dense Cluster

Molecular Characterization of Human Zyxin

Influence of different oxygen concentrations on mouse embryo development using time-lapse-imaging

Effects of opening the incubator on morphokinetics in mouse embryos

Human Sp4 transcription factor gene (SP4) maps to chromosome 7p15

Regional Localization of 725 Human Chromosome 7-Specific Yeast Artificial Chromosome Clones

The human S3a ribosomal protein: sequence, location and cell-free transcription of the functional gene

Human Sp3 Transcriptional Regulator Gene (SP3) Maps to Chromosome 2q31

Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: Not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individual

All known human H1 histone genes except the H10 gene are clustered on chromosome 6

Gene symbol: GLI3. Disease: Pallister-Hall syndrome

Gene symbol: GLI3. Disease: Greig cephalopolysyndactyly syndrome

Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality

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