P. Lukusa Tshilobo

发表

Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients

G. Matthijs, V. Racé, J. Muyembé-Tamfum, 2015, PloS one.

Skinfold over toenail is pathognomonic for the popliteal pterygium syndrome in a Congolese family with large intrafamilial variability

K. Devriendt, A. Lumaka, G. Mubungu, 2014, Clinical case reports.

Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator

H. Peeters, T. de Ravel, K. Devriendt, 2016, Clinical genetics.

Fragile X checklists: A meta‐analysis and development of a simplified universal clinical checklist

A. Lumaka, R. Hagerman, L. Mutesa, 2018, Molecular genetics & genomic medicine.

Clinical phenotypes and the biological parameters of Congolese patients suffering from sickle cell anemia: A first report from Central Africa

M. Aloni, P. Akilimali, T. M. Mikobi, 2017, Journal of clinical laboratory analysis.

Congenital lateral abdominal wall defect in two Congolese children.

K. Devriendt, A. Lumaka, G. Mubungu, 2019, Clinical dysmorphology.

A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family.

K. Devriendt, A. Lumaka, A. Corveleyn, 2014, European journal of medical genetics.

Meningocele in a Congolese Female with Beckwith-Wiedemann Phenotype

K. Devriendt, A. Lumaka, P. Lukusa Tshilobo, 2014, Case reports in genetics.

Preaxial Polydactyly of the Foot: Variable Expression of Trisomy 13 in a Case from Central Africa

K. Devriendt, A. Lumaka, P. Lukusa Tshilobo, 2014, Case reports in genetics.

Anthropometric and aesthetic outcomes for the nasolabial region in 101 consecutive African children with unilateral cleft lip one year after repair using the anatomical subunit approximation technique.

K. Devriendt, H. Reychler, P. Lukusa Tshilobo, 2017, International journal of oral and maxillofacial surgery.

A novel heterozygous mutation of three consecutive nucleotides causing Apert syndrome in a Congolese family.

K. Devriendt, A. Lumaka, A. Corveleyn, 2014, European journal of medical genetics.