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Publications by L L Estabrooks
Molecular Characterisation of Chromosome 4p Deletions Resulting in Wolf-Hirschhorn Syndrome.
Journal of Medical Genetics
Genetics
Related publications
Clinical Utility Gene Card For: Wolf–Hirschhorn (4p-) Syndrome
European Journal of Human Genetics
Genetics
Paternal Origin of the De Novo Deleted Chromosome 4 in Wolf-Hirschhorn Syndrome.
Journal of Medical Genetics
Genetics
Meiotic Prophase I Defects in an Oligospermic Man With Wolf-Hirschhorn Syndrome With Ring Chromosome 4
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
WHSC1L1 (Wolf-Hirschhorn Syndrome Candidate 1 Like Gene 1)
Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer Research
Oncology
Genetics
Hematology
A Double Cryptic Chromosome Imbalance Is an Important Factor to Explain Phenotypic Variability in Wolf–Hirschhorn Syndrome
European Journal of Human Genetics
Genetics
Growth Charts for Wolf-Hirschhorn Syndrome (0–4 Years of Age)
European Journal of Pediatrics
Child Health
Pediatrics
Perinatology
De Novo Truncating Variant in NSD2gene Leading to Atypical Wolf-Hirschhorn Syndrome Phenotype
BMC Medical Genetics
Genetics
Experience of the Diagnosis and Observation of a Child With Wolf-Hirschhorn Syndrome
CHILD`S HEALTH
Comprehensive Analysis of Wolf–Hirschhorn Syndrome Using Array CGH Indicates a High Prevalence of Translocations
European Journal of Human Genetics
Genetics