Lipson MH - Search Results

1

Natural history of mosaic trisomy 14 syndrome.

Fujimoto A, Allanson J, Crowe CA, Lipson MH, Johnson VP. Fujimoto A, et al. Among authors: lipson mh. Am J Med Genet. 1992 Sep 15;44(2):189-96. doi: 10.1002/ajmg.1320440214. Am J Med Genet. 1992. PMID: 1456290 Review.

2

New autosomal dominant branchio-oculo-facial syndrome.

Fujimoto A, Lipson M, Lacro RV, Shinno NW, Boelter WD, Jones KL, Wilson MG. Fujimoto A, et al. Am J Med Genet. 1987 Aug;27(4):943-51. doi: 10.1002/ajmg.1320270422. Am J Med Genet. 1987. PMID: 3321995 Review.

3

Radiological findings in Hallermann-Streiff syndrome: report of five cases and a review of the literature.

Christian CL, Lachman RS, Aylsworth AS, Fujimoto A, Gorlin RJ, Lipson MH, Graham JM Jr. Christian CL, et al. Among authors: lipson mh. Am J Med Genet. 1991 Dec 15;41(4):508-14. doi: 10.1002/ajmg.1320410426. Am J Med Genet. 1991. PMID: 1776646 Review.

4

Trisomy 14 mosaicism syndrome.

Lipson MH. Lipson MH. Am J Med Genet. 1987 Mar;26(3):541-4. doi: 10.1002/ajmg.1320260305. Am J Med Genet. 1987. PMID: 3565467

5

Thanatophoric dysplasia type I with syndactyly.

Brodie SG, Kitoh H, Lipson M, Sifry-Platt M, Wilcox WR. Brodie SG, et al. Am J Med Genet. 1998 Nov 16;80(3):260-2. doi: 10.1002/(sici)1096-8628(19981116)80:3<260::aid-ajmg15>3.0.co;2-s. Am J Med Genet. 1998. PMID: 9843049

6

Genetic mapping of a locus for multiple epiphyseal dysplasia (EDM2) to a region of chromosome 1 containing a type IX collagen gene.

Briggs MD, Choi H, Warman ML, Loughlin JA, Wordsworth P, Sykes BC, Irven CM, Smith M, Wynne-Davies R, Lipson MH, et al. Briggs MD, et al. Among authors: lipson mh. Am J Hum Genet. 1994 Oct;55(4):678-84. Am J Hum Genet. 1994. PMID: 7942845 Free PMC article.

7

Expanding the phenotype: Four new cases and hope for treatment in Bachmann-Bupp syndrome.

VanSickle EA, Michael J, Bachmann AS, Rajasekaran S, Prokop JW, Kuzniecky R, Hofstede FC, Steindl K, Rauch A, Lipson MH, Bupp CP. VanSickle EA, et al. Among authors: lipson mh. Am J Med Genet A. 2021 Nov;185(11):3485-3493. doi: 10.1002/ajmg.a.62473. Epub 2021 Sep 3. Am J Med Genet A. 2021. PMID: 34477286 Free PMC article.

8

Severe lactic acidosis caused by a novel frame-shift mutation in mitochondrial-encoded cytochrome c oxidase subunit II.

Wong LJ, Dai P, Tan D, Lipson M, Grix A, Sifry-Platt M, Gropman A, Chen TJ. Wong LJ, et al. Am J Med Genet. 2001 Jul 22;102(1):95-9. doi: 10.1002/1096-8628(20010722)102:1<95::aid-ajmg1412>3.0.co;2-u. Am J Med Genet. 2001. PMID: 11471180

9

Diverse mutations in the gene for cartilage oligomeric matrix protein in the pseudoachondroplasia-multiple epiphyseal dysplasia disease spectrum.

Briggs MD, Mortier GR, Cole WG, King LM, Golik SS, Bonaventure J, Nuytinck L, De Paepe A, Leroy JG, Biesecker L, Lipson M, Wilcox WR, Lachman RS, Rimoin DL, Knowlton RG, Cohn DH. Briggs MD, et al. Am J Hum Genet. 1998 Feb;62(2):311-9. doi: 10.1086/301713. Am J Hum Genet. 1998. PMID: 9463320 Free PMC article.

10

Prenatal diagnosis of asphyxiating thoracic dysplasia.

Lipson M, Waskey J, Rice J, Adomian G, Lachman R, Filly R, Rimoin D. Lipson M, et al. Am J Med Genet. 1984 Jun;18(2):273-7. doi: 10.1002/ajmg.1320180211. Am J Med Genet. 1984. PMID: 6540520

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

66 results

Search Page

Filters