Millan S Patel

8PUBLICATIONS
34CO-AUTHORS
Haematological tumoursNeurogeneticsGenetically modified animalsCancer geneticsGene mapping
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Publications (8)

|Oct 30, 2025
Missense variants in homeobox domain of PBX1 cause coracoclavicular ankylosis.

Maki Iwai, Kyra E Stuurman, Kirsten Meagher

|Mar 03, 2023
NOTCH1 loss of the TAD and PEST domain: An antimorph?

Pierre Boerkoel, Stephanie Huynh, Gui Xiang Yang

|Nov 01, 2022
Lethal respiratory course and additional features expand the phenotypic spectrum of PIEZO2-related distal arthrogryposis type 5.

Agata Oliwa, Glenda Hendson, Cheryl Longman

|Jan 12, 2022
Prevalence of ocular anomalies is increased in women with polycystic ovary syndrome-exploration of association with PAX6 genotype.

Zheyuan Zong, Shirin Kalyan, Cameron Andres

|Oct 26, 2021
Somatic mosaicism detected by genome-wide sequencing in 500 parent-child trios with suspected genetic disease: clinical and genetic counseling implications.

Courtney B Cook, Linlea Armstrong, Cornelius F Boerkoel

|May 04, 2021
New cases that expand the genotypic and phenotypic spectrum of Congenital NAD Deficiency Disorder.

Justin O Szot, Anne Slavotinek, Karen Chong

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Frequent Collaborators

2 joint publications

Alison M Elliott

1 joint publications

Yi Ariel Liu

1 joint publications

Anna F Lee

1 joint publications

Justin O Szot