Lachman RS - Search Results

1

Omphalocele with absent radial ray (ORR): a case with diploid-triploid mixoploidy.

Lin HJ, Schaber B, Hashimoto CH, Barajas L, Beall MH, Lachman RS. Lin HJ, et al. Among authors: lachman rs. Am J Med Genet. 1998 Jan 23;75(3):235-9. Am J Med Genet. 1998. PMID: 9475588 Review.

2

DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.

Lin HJ, Kakkis ED, Eteson DJ, Lachman RS. Lin HJ, et al. Among authors: lachman rs. Am J Med Genet. 1993 Sep 15;47(4):534-9. doi: 10.1002/ajmg.1320470419. Am J Med Genet. 1993. PMID: 8256819

3

Occipital encephalocele and MURCS association: case report and review of central nervous system anomalies in MURCS patients.

Lin HJ, Cornford ME, Hu B, Rutgers JK, Beall MH, Lachman RS. Lin HJ, et al. Among authors: lachman rs. Am J Med Genet. 1996 Jan 2;61(1):59-62. doi: 10.1002/(SICI)1096-8628(19960102)61:1<59::AID-AJMG11>3.0.CO;2-V. Am J Med Genet. 1996. PMID: 8741919 Review.

4

Anomalous inferior and superior venae cavae with oculoauriculovertebral defect: review of Goldenhar complex and malformations of left-right asymmetry.

Lin HJ, Owens TR, Sinow RM, Fu PC Jr, DeVito A, Beall MH, Lachman RS. Lin HJ, et al. Among authors: lachman rs. Am J Med Genet. 1998 Jan 6;75(1):88-94. doi: 10.1002/(sici)1096-8628(19980106)75:1<88::aid-ajmg18>3.0.co;2-o. Am J Med Genet. 1998. PMID: 9450864 Review.

5

Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: case report and review of triplications and their possible mechanism.

Wang J, Reddy KS, Wang E, Halderman L, Morgan BL, Lachman RS, Lin HJ, Cornford ME. Wang J, et al. Among authors: lachman rs. Am J Med Genet. 1999 Feb 12;82(4):312-7. doi: 10.1002/(sici)1096-8628(19990212)82:4<312::aid-ajmg7>3.0.co;2-9. Am J Med Genet. 1999. PMID: 10051164 Review.

6

Microdontia with severe microcephaly and short stature in two brothers: osteodysplastic primordial dwarfism with dental findings.

Lin HJ, Sue GY, Berkowitz CD, Brasel JA, Lachman RS. Lin HJ, et al. Among authors: lachman rs. Am J Med Genet. 1995 Aug 28;58(2):136-42. doi: 10.1002/ajmg.1320580209. Am J Med Genet. 1995. PMID: 8533804 Review.

7

New mesomelic dysplasia with absent fibulae and triangular tibiae.

Savarirayan R, Cormier-Daire V, Curry CJ, Nashelsky MB, Rappaport V, Rimoin DL, Lachman RS. Savarirayan R, et al. Among authors: lachman rs. Am J Med Genet. 2000 Sep 4;94(1):59-63. doi: 10.1002/1096-8628(20000904)94:1<59::aid-ajmg12>3.0.co;2-2. Am J Med Genet. 2000. PMID: 10982484

8

Radiographic and morphologic findings in a previously undescribed type of mesomelic dysplasia resembling atelosteogenesis type II.

Brodie SG, Lachman RS, Crandall BF, Fox MA, Rimoin DL, Cohn DH, Wilcox WR. Brodie SG, et al. Among authors: lachman rs. Am J Med Genet. 1998 Nov 16;80(3):247-51. Am J Med Genet. 1998. PMID: 9843047

9

Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene.

Graham JM Jr, Braddock SR, Mortier GR, Lachman R, Van Dop C, Jabs EW. Graham JM Jr, et al. Am J Med Genet. 1998 May 26;77(4):322-9. doi: 10.1002/(sici)1096-8628(19980526)77:4<322::aid-ajmg14>3.0.co;2-k. Am J Med Genet. 1998. PMID: 9600744

10

Gracile bone dysplasia.

Thomas JA, Rimoin DL, Lachman RS, Wilcox WR. Thomas JA, et al. Among authors: lachman rs. Am J Med Genet. 1998 Jan 6;75(1):95-100. Am J Med Genet. 1998. PMID: 9450865

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

281 results

Search Page

Filters