Dr. Barbara Rose Pober MD
Pediatrician
185 Cambridge St, Rm 222 Partners Center For Boston MA, 02114About
Dr. Barbara Pober is a pediatrician practicing in Boston, MA. Dr. Pober is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Pober diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Pober can oversee and manage the physical, mental and emotional health of their patients.
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Early puberty in Williams syndrome.
- 46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters.
- Truncating mutations in FOXC2 cause multiple lymphedema syndromes.
- Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophy.
- Differences by sex in cardiovascular disease in Williams syndrome.
- Unknown syndrome in sibs: pili torti, growth delay, developmental delay, and mild neurological abnormalities.
- FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6.
- Multisystem study of 20 older adults with Williams syndrome.
- Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.
- Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement.
- Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH.
- Congenital diaphragmatic hernia and associated cardiovascular malformations: type, frequency, and impact on management.
- Congenital diaphragmatic hernia and pulmonary hypoplasia: new insights from developmental biology and genetics.
- Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.
- Nutrient intakes in women and congenital diaphragmatic hernia in their offspring.
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Nearby Providers
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