Mahin Golabi

Mahin Golabi

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Mahin Golabi

Mahin Golabi

Publications by authors named "Mahin Golabi"

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A new case of a LUMBAR syndrome.

Am J Med Genet A 2014 Jan 20;164A(1):204-7. Epub 2013 Nov 20.

Division of Medical Genetics, California Pacific Medical Center, San Francisco, California.

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http://dx.doi.org/10.1002/ajmg.a.36215DOI Listing
January 2014

Novel duplication in glypican-4 as an apparent cause of Simpson-Golabi-Behmel syndrome.

Am J Med Genet A 2010 Dec;152A(12):3179-81

Division of Medical Genetics, Children's Hospital & Research Center Oakland, Oakland, California 94609, USA.

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http://dx.doi.org/10.1002/ajmg.a.33450DOI Listing
December 2010

Tissue-limited mosaicism for monosomy 13.

Am J Med Genet A 2010 Oct;152A(10):2634-9

California Pacific Medical Center and San Francisco General Hospital, School of Medicine, University of California San Francisco, San Francisco, California, USA.

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http://dx.doi.org/10.1002/ajmg.a.33651DOI Listing
October 2010

Novel FGFR2 deletion in a patient with Beare-Stevenson-like syndrome.

Am J Med Genet A 2009 Aug;149A(8):1814-7

Department of Pediatrics, University of California, San Francisco, 94143-0748, USA.

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http://dx.doi.org/10.1002/ajmg.a.32947DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2785435PMC
August 2009

Gardner-Silengo-Wachtel or genito-palato-cadiac syndrome with associated autosomal aneuploidy.

Am J Med Genet A 2009 Feb;149A(4):693-7

California Pacific Medical Center, San Francisco, California, USA.

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http://dx.doi.org/10.1002/ajmg.a.32755DOI Listing
February 2009

DOOR syndrome: clinical report, literature review and discussion of natural history.

Am J Med Genet A 2007 Dec;143A(23):2821-31

School of Medicine, University of California, San Francisco, California.

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http://dx.doi.org/10.1002/ajmg.a.32054DOI Listing
December 2007

Bifid tongue: a rare feature associated with infants of diabetic mother syndrome.

Am J Med Genet A 2007 Sep;143A(17):2035-9

University of California, San Francisco, California, USA.

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http://dx.doi.org/10.1002/ajmg.a.31877DOI Listing
September 2007

Marinesco-Sjögren syndrome in a male with mild dysmorphism.

Am J Med Genet A 2005 Mar;133A(2):197-201

Department of Pediatrics, Division of Medical Genetics, University of California-San Francisco, 533 Parnassus Street, San Francisco, CA 94143-0748, USA.

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http://doi.wiley.com/10.1002/ajmg.a.30504
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http://dx.doi.org/10.1002/ajmg.a.30504DOI Listing
March 2005

A tribute to Bryan D. Hall: Festschrift 2003.

Am J Med Genet A 2003 Nov;123A(1):1-4

Deparment of Pediatrics, University of Utah Health Sciences Center, Salt Lake City, Utah, USA.

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http://dx.doi.org/10.1002/ajmg.a.20499DOI Listing
November 2003

Fertility in a female with mosaic trisomy 8.

Fertil Steril 2003 Jan;79(1):206-8

Division of Medical Genetics, Department of Pediatrics, University of California San Francisco, San Francisco, California, USA.

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http://dx.doi.org/10.1016/s0015-0282(02)04410-2DOI Listing
January 2003

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.

Hum Genet 2002 Apr 2;110(4):297-301. Epub 2002 Mar 2.

Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.

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http://dx.doi.org/10.1007/s00439-002-0695-5DOI Listing
April 2002