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Blood
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April 22, 2017
MDS with isolated del(5q) and internuclear bridging
Zhaodong Xu, Jean McGowan-Jordan
Blood
|
January 17, 2017
CML with complex chromosome rearrangements and dysplastic megakaryocytes
Zhaodong Xu, Jean McGowan-Jordan
Cytogenetic and Genome Research
|
July 30, 2023
Addenda to ISCN 2020
Ros Hastings, Jean McGowan-Jordan, Sarah Moore, et al.
Cytogenetic and Genome Research
|
August 18, 2021
Re: International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts, by T. Liehr
Jean McGowan-Jordan, Ros Hastings, Sarah Moore
Cancer Genetics
|
October 14, 2017
A rare case of pediatric lipoma with t(9;12)(p22;q14) and evidence of HMGA2-NFIB gene fusion
Melanie Lacaria, Dina El Demellawy, Jean McGowan-Jordan
Prenatal Diagnosis
|
April 19, 2011
The detection of chromosome anomalies by QF-PCR and residual risks as compared to G-banded analysis
Marsha D Speevak, Jean McGowan-Jordan, Kathy Chun
American Journal of Medical Genetics. Part A
|
May 16, 2012
Novel clinical findings in a case of postnatally diagnosed trisomy 12 mosaicism
Walla Al-Hertani, Jean McGowan-Jordan, Judith E Allanson
American Journal of Medical Genetics. Part A
|
December 12, 2002
De novo dup(X)(q22.3q26) in a girl with evidence that functional disomy of X material is the cause of her abnormal phenotype
Linlea Armstrong, Jean McGowan-Jordan, Kathleen Brierley, et al.
European Journal of Medical Genetics
|
April 3, 2025
Familial inheritance of 14q terminal deletion syndrome and review of the literature
Krista M Vincent, Bradley Prince, Jean McGowan-Jordan, et al.
Pathology
|
March 4, 2017
Update on molecular findings in rhabdomyosarcoma
Dina El Demellawy, Jean McGowan-Jordan, Joseph de Nanassy, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
Blood
|
April 22, 2017
MDS with isolated del(5q) and internuclear bridging
Zhaodong Xu, Jean McGowan-Jordan
Blood
|
January 17, 2017
CML with complex chromosome rearrangements and dysplastic megakaryocytes
Zhaodong Xu, Jean McGowan-Jordan
Cytogenetic and Genome Research
|
July 30, 2023
Addenda to ISCN 2020
Ros Hastings, Jean McGowan-Jordan, Sarah Moore, et al.
Cytogenetic and Genome Research
|
August 18, 2021
Re: International System for Human Cytogenetic or Cytogenomic Nomenclature (ISCN): Some Thoughts, by T. Liehr
Jean McGowan-Jordan, Ros Hastings, Sarah Moore
Cancer Genetics
|
October 14, 2017
A rare case of pediatric lipoma with t(9;12)(p22;q14) and evidence of HMGA2-NFIB gene fusion
Melanie Lacaria, Dina El Demellawy, Jean McGowan-Jordan
Prenatal Diagnosis
|
April 19, 2011
The detection of chromosome anomalies by QF-PCR and residual risks as compared to G-banded analysis
Marsha D Speevak, Jean McGowan-Jordan, Kathy Chun
American Journal of Medical Genetics. Part A
|
May 16, 2012
Novel clinical findings in a case of postnatally diagnosed trisomy 12 mosaicism
Walla Al-Hertani, Jean McGowan-Jordan, Judith E Allanson
American Journal of Medical Genetics. Part A
|
December 12, 2002
De novo dup(X)(q22.3q26) in a girl with evidence that functional disomy of X material is the cause of her abnormal phenotype
Linlea Armstrong, Jean McGowan-Jordan, Kathleen Brierley, et al.
European Journal of Medical Genetics
|
April 3, 2025
Familial inheritance of 14q terminal deletion syndrome and review of the literature
Krista M Vincent, Bradley Prince, Jean McGowan-Jordan, et al.
Pathology
|
March 4, 2017
Update on molecular findings in rhabdomyosarcoma
Dina El Demellawy, Jean McGowan-Jordan, Joseph de Nanassy, et al.
Page
of 4