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1

Medical genetics: advances in brief: Girls with fragile X syndrome: physical and neurocognitive status and outcome by Goodship, Judith

Published 1992

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Medical genetics: advances in brief: Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion by Goodship, Judith

Published 1992

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Medical genetics: advances in brief: Familial case with sequence variant in the testis-determining region associated with two sex phenotypes by Goodship, Judith

Published 1992

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Medical genetics: advances in brief: Recombination of 4p16 DNA markers in an unusual family with Huntington disease by Goodship, Judith

Published 1992

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Medical genetics: advances in brief by Goodship, Judith

Published 1992

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Medical genetics: advances in brief: A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening by Goodship, Judith

Published 1993

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Medical genetics: advances in brief: Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism by Goodship, Judith

Published 1993

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Medical genetics: advances in brief: Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COLIA2 locus by Goodship, Judith

Published 1993

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Medical genetics: advances in brief: Rubinstein-Taybi syndrome caused by submicroscopic deletions with 16p13.3 by Goodship, Judith

Published 1993

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Medical genetics: advances in brief: X-linked borderline mental retardation with prominent behavioural disturbance: phenotype, genetic localization, and evidence for disturbed mono... by Goodship, Judith

Published 1993

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11

Autozygosity Mapping of a Seckel Syndrome Locus to Chromosome 3q22.1-q24 by Goodship, Judith, Gill, Harinder, Carter, Joan, Jackson, Andrew, Splitt, Miranda, Wright, Michael

Published 2000

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A wide spectrum of phenotypes in a family with renal coloboma syndrome caused by a PAX2 mutation by Adam, Jennifer, Browning, Andrew C., Vaideanu, Daniela, Heidet, Laurence, Goodship, Judith A., Sayer, John A.

Published 2013

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Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA) by Muncke, Nadja, Niesler, Beate, Roeth, Ralph, Schön, Karin, Rüdiger, Heinz-Juergen, Goldmuntz, Elizabeth, Goodship, Judith, Rappold, Gudrun

Published 2005

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Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation by Howey, Richard, Mamasoula, Chrysovalanto, Töpf, Ana, Nudel, Ron, Goodship, Judith A., Keavney, Bernard D., Cordell, Heather J.

Published 2015

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15

Using population data for assessing next-generation sequencing performance by Houniet, Darren T., Rahman, Thahira J., Al Turki, Saeed, Hurles, Matthew E., Xu, Yaobo, Goodship, Judith, Keavney, Bernard, Santibanez Koref, Mauro

Published 2015

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16

Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleus by Blair, Helen J, Tompson, Stuart, Liu, Yu-Ning, Campbell, Jennifer, MacArthur, Katie, Ponting, Chris P, Ruiz-Perez, Victor L, Goodship, Judith A

Published 2011

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Inversin/Nephrocystin-2 Is Required for Fibroblast Polarity and Directional Cell Migration by Veland, Iben R., Montjean, Rodrick, Eley, Lorraine, Pedersen, Lotte B., Schwab, Albrecht, Goodship, Judith, Kristiansen, Karsten, Pedersen, Stine F., Saunier, Sophie, Christensen, Søren T.

Published 2013

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18

A Nonsense Mutation in the IKBKG Gene in Mares with Incontinentia Pigmenti by Towers, Rachel E., Murgiano, Leonardo, Millar, David S., Glen, Elise, Topf, Ana, Jagannathan, Vidhya, Drögemüller, Cord, Goodship, Judith A., Clarke, Angus J., Leeb, Tosso

Published 2013

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19

Determining the Population Frequency of the CFHR3/CFHR1 Deletion at 1q32 by Holmes, Lucy V., Strain, Lisa, Staniforth, Scott J., Moore, Iain, Marchbank, Kevin, Kavanagh, David, Goodship, Judith A., Cordell, Heather J., Goodship, Timothy H. J.

Published 2013

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20

Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition by Richards, Anna, Buddles, Mark R., Donne, Rosemary L., Kaplan, Bernard S., Kirk, Edwin, Venning, Michael C., Tielemans, Christian L., Goodship, Judith A., Goodship, Timothy H. J.

Published 2001

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Search Results - Goodship, Judith

Medical genetics: advances in brief: Girls with fragile X syndrome: physical and neurocognitive status and outcome by Goodship, Judith

Medical genetics: advances in brief: Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion by Goodship, Judith

Medical genetics: advances in brief: Familial case with sequence variant in the testis-determining region associated with two sex phenotypes by Goodship, Judith

Medical genetics: advances in brief: Recombination of 4p16 DNA markers in an unusual family with Huntington disease by Goodship, Judith

Medical genetics: advances in brief by Goodship, Judith

Medical genetics: advances in brief: A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening by Goodship, Judith

Medical genetics: advances in brief: Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism by Goodship, Judith

Medical genetics: advances in brief: Partial isodisomy for maternal chromosome 7 and short stature in an individual with a mutation at the COLIA2 locus by Goodship, Judith

Medical genetics: advances in brief: Rubinstein-Taybi syndrome caused by submicroscopic deletions with 16p13.3 by Goodship, Judith

Medical genetics: advances in brief: X-linked borderline mental retardation with prominent behavioural disturbance: phenotype, genetic localization, and evidence for disturbed mono... by Goodship, Judith

Autozygosity Mapping of a Seckel Syndrome Locus to Chromosome 3q22.1-q24 by Goodship, Judith, Gill, Harinder, Carter, Joan, Jackson, Andrew, Splitt, Miranda, Wright, Michael

A wide spectrum of phenotypes in a family with renal coloboma syndrome caused by a PAX2 mutation by Adam, Jennifer, Browning, Andrew C., Vaideanu, Daniela, Heidet, Laurence, Goodship, Judith A., Sayer, John A.

Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA) by Muncke, Nadja, Niesler, Beate, Roeth, Ralph, Schön, Karin, Rüdiger, Heinz-Juergen, Goldmuntz, Elizabeth, Goodship, Judith, Rappold, Gudrun

Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation by Howey, Richard, Mamasoula, Chrysovalanto, Töpf, Ana, Nudel, Ron, Goodship, Judith A., Keavney, Bernard D., Cordell, Heather J.

Using population data for assessing next-generation sequencing performance by Houniet, Darren T., Rahman, Thahira J., Al Turki, Saeed, Hurles, Matthew E., Xu, Yaobo, Goodship, Judith, Keavney, Bernard, Santibanez Koref, Mauro

Evc2 is a positive modulator of Hedgehog signalling that interacts with Evc at the cilia membrane and is also found in the nucleus by Blair, Helen J, Tompson, Stuart, Liu, Yu-Ning, Campbell, Jennifer, MacArthur, Katie, Ponting, Chris P, Ruiz-Perez, Victor L, Goodship, Judith A

Inversin/Nephrocystin-2 Is Required for Fibroblast Polarity and Directional Cell Migration by Veland, Iben R., Montjean, Rodrick, Eley, Lorraine, Pedersen, Lotte B., Schwab, Albrecht, Goodship, Judith, Kristiansen, Karsten, Pedersen, Stine F., Saunier, Sophie, Christensen, Søren T.

A Nonsense Mutation in the IKBKG Gene in Mares with Incontinentia Pigmenti by Towers, Rachel E., Murgiano, Leonardo, Millar, David S., Glen, Elise, Topf, Ana, Jagannathan, Vidhya, Drögemüller, Cord, Goodship, Judith A., Clarke, Angus J., Leeb, Tosso

Determining the Population Frequency of the CFHR3/CFHR1 Deletion at 1q32 by Holmes, Lucy V., Strain, Lisa, Staniforth, Scott J., Moore, Iain, Marchbank, Kevin, Kavanagh, David, Goodship, Judith A., Cordell, Heather J., Goodship, Timothy H. J.

Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition by Richards, Anna, Buddles, Mark R., Donne, Rosemary L., Kaplan, Bernard S., Kirk, Edwin, Venning, Michael C., Tielemans, Christian L., Goodship, Judith A., Goodship, Timothy H. J.

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