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Author/Creator Graham, John M.

1. A standard of care for individuals with PIK3CA‐related disorders: An international expert consensus statement. Issue 1 (16th July 2021)

Authors:
Douzgou, Sofia; Rawson, Myfanwy; Baselga, Eulalia; Danielpour, Moise; Faivre, Laurence; Kashanian, Alon; Keppler‐Noreuil, Kim M.; Kuentz, Paul; Mancini, Grazia M. S.; Maniere, Marie‐Cecile; Martinez‐Glez, Victor; Parker, Victoria E.; Semple, Robert K.; Srivastava, Siddharth; Vabres, Pierre; De Wi...
Journal:
Clinical genetics
Issue:
Volume 101:Issue 1(2022)
Page Start:
32
Record Type:
Journal Article
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2. A syndrome of facial dysmorphism, cubital pterygium, short distal phalanges, swan neck deformity of fingers, and scoliosis. Issue 4 (23rd January 2014)

Authors:
Girisha, Katta M.; Abdollahpour, Hengameh; Shah, Hitesh; Bhavani, Gandham SriLakshmi; Graham, John M.; Boggula, Vijay Raju; Phadke, Shubha R.; Kutsche, Kerstin
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 4(2014.)
Page Start:
1035
Record Type:
Journal Article
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4. Approach to overgrowth syndromes in the genome era. Issue 4 (2nd December 2019)

Authors:
Burkardt, Deepika D.; Tatton‐Brown, Katrina; Dobyns, William; Graham, John M.
Other Names:
Burkardt Deepika guestEditor.; Tatton‐Brown Kate guestEditor.; Dobyns William B. guestEditor.; Graham John guestEditor.
Journal:
American journal of medical genetics
Issue:
Volume 181:Issue 4(2019)
Page Start:
483
Record Type:
Journal Article
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5. Clinical delineation and natural history of the PIK3CA‐related overgrowth spectrum. Issue 7 (29th April 2014)

Authors:
Keppler‐Noreuil, Kim M.; Sapp, Julie C.; Lindhurst, Marjorie J.; Parker, Victoria E.R.; Blumhorst, Cathy; Darling, Thomas; Tosi, Laura L.; Huson, Susan M.; Whitehouse, Richard W.; Jakkula, Eveliina; Grant, Ian; Balasubramanian, Meena; Chandler, Kate E.; Fraser, Jamie L.; Gucev, Zoran; Crow, Yanic...
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 7(2014.)
Page Start:
1713
Record Type:
Journal Article
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6. Clinical management of patients with ASXL1 mutations and Bohring–Opitz syndrome, emphasizing the need for Wilms tumor surveillance. (29th April 2015)

Authors:
Russell, Bianca; Johnston, Jennifer J.; Biesecker, Leslie G.; Kramer, Nancy; Pickart, Angela; Rhead, William; Tan, Wen‐Hann; Brownstein, Catherine A.; Kate Clarkson, L.; Dobson, Amy; Rosenberg, Avi Z.; Vergano, Samantha A. Schrier; Helm, Benjamin M.; Harrison, Rachel E.; Graham, John M.
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 9(2015:Sep.)
Page Start:
2122
Record Type:
Journal Article
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7. Coffin–Siris Syndrome and the BAF Complex: Genotype–Phenotype Study in 63 Patients. Issue 11 (30th August 2013)

Authors:
Santen, Gijs W.E.; Aten, Emmelien; Vulto‐van Silfhout, Anneke T.; Pottinger, Caroline; van Bon, Bregje W.M.; van Minderhout, Ivonne J.H.M.; Snowdowne, Ronelle; van der Lans, Christian A.C.; Boogaard, Merel; Linssen, Margot M.L.; Vijfhuizen, Linda; van der Wielen, Michiel J.R.; Vollebregt, M.J. (E...
Journal:
Human mutation
Issue:
Volume 34:Issue 11(2013:Nov.)
Page Start:
1519
Record Type:
Journal Article
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8. Coffin–Siris Syndrome and the BAF Complex: Genotype–Phenotype Study in 63 Patients. Issue 11 (30th August 2013)

Authors:
Santen, Gijs W.E.; Aten, Emmelien; Vulto‐van Silfhout, Anneke T.; Pottinger, Caroline; van, Bregje W.M.; van, Ivonne J.H.M.; Snowdowne, Ronelle; van der, Christian A.C.; Boogaard, Merel; Linssen, Margot M.L.; Vijfhuizen, Linda; van der, Michiel J.R.; Vollebregt, M.J. (Ellen); Breuning, Martijn H....
Journal:
Human mutation
Issue:
Volume 34:Issue 11(2013:Nov.)
Page Start:
1519
Record Type:
Journal Article
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10. Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome. Issue 6 (30th March 2021)

Authors:
Sheppard, Sarah E.; Campbell, Ian M.; Harr, Margaret H.; Gold, Nina; Li, Dong; Bjornsson, Hans T.; Cohen, Julie S.; Fahrner, Jill A.; Fatemi, Ali; Harris, Jacqueline R.; Nowak, Catherine; Stevens, Cathy A.; Grand, Katheryn; Au, Margaret; Graham, John M.; Sanchez‐Lara, Pedro A.; Campo, Miguel Del;...
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 6(2021)
Page Start:
1649
Record Type:
Journal Article
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