Robinow syndrome without mesomelic 'brachymelia': a report of five cases.

Author:

Bain M D,Winter R M,Burn J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. A newly recognised dwarfing syndrome;Robinow, M.; Silverman, F.N.; Smith, H.D.;Am J Dis Child,1969

2. Male to male transmissions of Robinow's syndrome;Shprintzen, R.; Goldberg, R.; Saenger, P.; Sidoti, E.;Am J Dis Child,1982

3. Syndrome de Robinow a transmission dominante;Vallee, L.; Van Nerom, P.Y.; Ferraz, F.G.;Arch Fr Pediatr,1982

4. Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome). A new genetic entity?;Wadia, R.S.; Shirole, D.B.; Dikshit, M.S.;J Med Genet,1978

5. Covesdem syndrome;Wadia, R.S.;J Med Genet,1979

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1. Obstetrical Challenges in Robinow Syndrome;Case Reports in Obstetrics and Gynecology;2022-07-22

2. Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux;Journal of the American Society of Nephrology;2021-02-17

3. Craniofacial phenotypes associated with Robinow syndrome;American Journal of Medical Genetics Part A;2020-11-25

4. Extremity anomalies associated with Robinow syndrome;American Journal of Medical Genetics Part A;2020-09-25

5. 50 years of Robinow syndrome;American Journal of Medical Genetics Part A;2020-07-21

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