Rosenbaum KN - Search Results

1

Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

Stern HJ, Saal HM, Lee JS, Fain PR, Goldgar DE, Rosenbaum KN, Barker DF. Stern HJ, et al. Among authors: rosenbaum kn. J Med Genet. 1992 Mar;29(3):184-7. doi: 10.1136/jmg.29.3.184. J Med Genet. 1992. PMID: 1348094 Free PMC article.

2

New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters.

Kaler SG, Garrity AM, Stern HJ, Rosenbaum KN, Orrison BM, Marini JC, Bernardini I, Saal HM. Kaler SG, et al. Among authors: rosenbaum kn. Am J Med Genet. 1992 Aug 1;43(6):983-8. doi: 10.1002/ajmg.1320430615. Am J Med Genet. 1992. PMID: 1415349

3

Patient with craniosynostosis and marfanoid phenotype (Shprintzen-Goldberg syndrome) and cloverleaf skull.

Saal HM, Bulas DI, Allen JF, Vezina LG, Walton D, Rosenbaum KN. Saal HM, et al. Among authors: rosenbaum kn. Am J Med Genet. 1995 Jul 17;57(4):573-8. doi: 10.1002/ajmg.1320570411. Am J Med Genet. 1995. PMID: 7573131 Review.

4

Brachmann-de Lange syndrome with normal IQ.

Saal HM, Samango-Sprouse CA, Rodnan LA, Rosenbaum KN, Custer DA. Saal HM, et al. Among authors: rosenbaum kn. Am J Med Genet. 1993 Nov 15;47(7):995-8. doi: 10.1002/ajmg.1320470711. Am J Med Genet. 1993. PMID: 8291543 Review.

5

Neurodevelopmental profile of infants and toddlers with oculo-auriculo-vertebral spectrum and the correlation of prognosis with physical findings.

Cohen MS, Samango-Sprouse CA, Stern HJ, Custer DA, Vaught DR, Saal HM, Tifft CJ, Rosenbaum KN. Cohen MS, et al. Among authors: rosenbaum kn. Am J Med Genet. 1995 Dec 18;60(6):535-40. doi: 10.1002/ajmg.1320600610. Am J Med Genet. 1995. PMID: 8825891

6

Progressive occlusive cerebrovascular disease in a patient with neurofibromatosis type 1.

Gorelick MH, Powell CM, Rosenbaum KN, Saal HM, Conry J, Fitz CR. Gorelick MH, et al. Among authors: rosenbaum kn. Clin Pediatr (Phila). 1992 May;31(5):313-5. doi: 10.1177/000992289203100511. Clin Pediatr (Phila). 1992. PMID: 1582101 No abstract available.

7

Screening the newborn for anatomic and metabolic defects.

Saal HM, Rosenbaum KN. Saal HM, et al. Among authors: rosenbaum kn. Pediatr Ann. 1988 Jul;17(7):467, 470-2, 474-6. doi: 10.3928/0090-4481-19880701-09. Pediatr Ann. 1988. PMID: 2969500 No abstract available.

8

Prenatal diagnosis of Pallister-Killian syndrome: resolution of cytogenetic ambiguity by use of fluorescent in situ hybridization.

McLean S, Stanley W, Stern H, Fonda-Allen J, Devine G, Ellingham T, Rosenbaum K. McLean S, et al. Prenat Diagn. 1992 Dec;12(12):985-91. doi: 10.1002/pd.1970121203. Prenat Diagn. 1992. PMID: 1287646

9

Middle ear disease in childhood achondroplasia.

Berkowitz RG, Grundfast KM, Scott C, Saal H, Stern H, Rosenbaum K. Berkowitz RG, et al. Ear Nose Throat J. 1991 May;70(5):305-8. Ear Nose Throat J. 1991. PMID: 1914954 No abstract available.

10

Variable prenatal appearance of osteogenesis imperfecta.

Bulas DI, Stern HJ, Rosenbaum KN, Fonda JA, Glass RB, Tifft C. Bulas DI, et al. Among authors: rosenbaum kn. J Ultrasound Med. 1994 Jun;13(6):419-27. doi: 10.7863/jum.1994.13.6.419. J Ultrasound Med. 1994. PMID: 8083940

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

69 results

Search Page