Warman ML - Search Results

1

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis.

Jabs EW, Müller U, Li X, Ma L, Luo W, Haworth IS, Klisak I, Sparkes R, Warman ML, Mulliken JB, et al. Jabs EW, et al. Among authors: warman ml. Cell. 1993 Nov 5;75(3):443-50. doi: 10.1016/0092-8674(93)90379-5. Cell. 1993. PMID: 8106171

2

Newly recognized autosomal dominant disorder with craniosynostosis.

Warman ML, Mulliken JB, Hayward PG, Müller U. Warman ML, et al. Am J Med Genet. 1993 Jun 1;46(4):444-9. doi: 10.1002/ajmg.1320460420. Am J Med Genet. 1993. PMID: 8357019

3

Assignment of a gene locus involved in craniosynostosis to chromosome 5qter.

Müller U, Warman ML, Mulliken JB, Weber JL. Müller U, et al. Among authors: warman ml. Hum Mol Genet. 1993 Feb;2(2):119-22. doi: 10.1093/hmg/2.2.119. Hum Mol Genet. 1993. PMID: 8499900

4

Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2.

Vikkula M, Boon LM, Carraway KL 3rd, Calvert JT, Diamonti AJ, Goumnerov B, Pasyk KA, Marchuk DA, Warman ML, Cantley LC, Mulliken JB, Olsen BR. Vikkula M, et al. Among authors: warman ml. Cell. 1996 Dec 27;87(7):1181-90. doi: 10.1016/s0092-8674(00)81814-0. Cell. 1996. PMID: 8980225 Free article.

5

Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family.

Mundlos S, Mulliken JB, Abramson DL, Warman ML, Knoll JH, Olsen BR. Mundlos S, et al. Among authors: warman ml. Hum Mol Genet. 1995 Jan;4(1):71-5. doi: 10.1093/hmg/4.1.71. Hum Mol Genet. 1995. PMID: 7711736

6

A gene for familial venous malformations maps to chromosome 9p in a second large kindred.

Gallione CJ, Pasyk KA, Boon LM, Lennon F, Johnson DW, Helmbold EA, Markel DS, Vikkula M, Mulliken JB, Warman ML, et al. Gallione CJ, et al. Among authors: warman ml. J Med Genet. 1995 Mar;32(3):197-9. doi: 10.1136/jmg.32.3.197. J Med Genet. 1995. PMID: 7783168 Free PMC article.

7

Assignment of a locus for dominantly inherited venous malformations to chromosome 9p.

Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML. Boon LM, et al. Among authors: warman ml. Hum Mol Genet. 1994 Sep;3(9):1583-7. doi: 10.1093/hmg/3.9.1583. Hum Mol Genet. 1994. PMID: 7833915

8

Molecular genetics and craniofacial surgery.

Mulliken JB, Warman ML. Mulliken JB, et al. Among authors: warman ml. Plast Reconstr Surg. 1996 Mar;97(3):666-75. doi: 10.1097/00006534-199603000-00030. Plast Reconstr Surg. 1996. PMID: 8596804 Review. No abstract available.

9

Hemangioma in twins.

Cheung DS, Warman ML, Mulliken JB. Cheung DS, et al. Among authors: warman ml. Ann Plast Surg. 1997 Mar;38(3):269-74. doi: 10.1097/00000637-199703000-00014. Ann Plast Surg. 1997. PMID: 9088466

10

A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.

Boon LM, Brouillard P, Irrthum A, Karttunen L, Warman ML, Rudolph R, Mulliken JB, Olsen BR, Vikkula M. Boon LM, et al. Among authors: warman ml. Am J Hum Genet. 1999 Jul;65(1):125-33. doi: 10.1086/302450. Am J Hum Genet. 1999. PMID: 10364524 Free PMC article.

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