Bird LM - Search Results

1

Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.

Verscaj CP, Velez-Bartolomei F, Bodle E, Chan K, Lyons MJ, Thorson W, Tan WH, Rodig N, Graham JM Jr, Peron A, Quintero-Rivera F, Zackai EH, Thomas MA, Stevens CA, Adam MP, Bird LM, Jones MC, Matalon DR. Verscaj CP, et al. Among authors: bird lm. Prenat Diagn. 2024 Feb;44(2):237-246. doi: 10.1002/pd.6424. Epub 2023 Aug 26. Prenat Diagn. 2024. PMID: 37632214 Review.

2

Anterior cervical hypertrichosis: a dominantly inherited isolated defect.

Braddock SR, Jones KL, Bird LM, Villegas I, Jones MC. Braddock SR, et al. Among authors: bird lm. Am J Med Genet. 1995 Feb 13;55(4):498-9. doi: 10.1002/ajmg.1320550421. Am J Med Genet. 1995. PMID: 7762594 Review.

3

Recurrence of diaphragmatic agenesis associated with multiple midline defects: evidence for an autosomal gene regulating the midline.

Bird LM, Newbury RO, Ruiz-Velasco R, Jones MC. Bird LM, et al. Am J Med Genet. 1994 Oct 15;53(1):33-8. doi: 10.1002/ajmg.1320530108. Am J Med Genet. 1994. PMID: 7802033 Review.

4

Female infant with oncocytic cardiomyopathy and microphthalmia with linear skin defects (MLS): a clue to the pathogenesis of oncocytic cardiomyopathy?

Bird LM, Krous HF, Eichenfield LF, Swalwell CI, Jones MC. Bird LM, et al. Am J Med Genet. 1994 Nov 1;53(2):141-8. doi: 10.1002/ajmg.1320530205. Am J Med Genet. 1994. PMID: 7856638 Review.

5

Gram-negative bacteremia in four patients with Klippel-Trenaunay-Weber syndrome.

Bird LM, Jones MC, Kuppermann N, Huskins WC. Bird LM, et al. Pediatrics. 1996 May;97(5):739-41. Pediatrics. 1996. PMID: 8628620 No abstract available.

6

Anencephaly with holoprosencephalic facies due to ring chromosome 18.

Bird LM, Pretorius DH, Mendoza AE, Jones MC. Bird LM, et al. Clin Dysmorphol. 1997 Oct;6(4):351-8. doi: 10.1097/00019605-199710000-00009. Clin Dysmorphol. 1997. PMID: 9354845

7

Choroid plexus cysts in the mid-trimester fetus--practical application suggests superiority of an individualized risk method of counseling for trisomy 18.

Bird LM, Dixson B, Masser-Frye D, Mestre L, Ribas L, Mullen L, Kalla K, Carder K, Huslig M, Catanzarite VA, Jones MC. Bird LM, et al. Prenat Diagn. 2002 Sep;22(9):792-7. doi: 10.1002/pd.411. Prenat Diagn. 2002. PMID: 12224073

8

Neonatal phenotype in Kabuki syndrome.

Vaux KK, Hudgins L, Bird LM, Roeder E, Curry CJ, Jones M, Jones KL. Vaux KK, et al. Among authors: bird lm. Am J Med Genet A. 2005 Jan 30;132A(3):244-7. doi: 10.1002/ajmg.a.30336. Am J Med Genet A. 2005. PMID: 15690369

9

Megalourethra: A report of three cases associated with maternal diabetes and a review of the literature--is sonic hedgehog the common pathway?

Vaux KK, Jones MC, Benirschke K, Bird LM, Jones KL. Vaux KK, et al. Among authors: bird lm. Am J Med Genet A. 2005 Jan 30;132A(3):314-7. doi: 10.1002/ajmg.a.30286. Am J Med Genet A. 2005. PMID: 15690378 Review.

10

Oculocerebrocutaneous syndrome: the brain malformation defines a core phenotype.

Moog U, Jones MC, Bird LM, Dobyns WB. Moog U, et al. Among authors: bird lm. J Med Genet. 2005 Dec;42(12):913-21. doi: 10.1136/jmg.2005.031369. Epub 2005 May 6. J Med Genet. 2005. PMID: 15879499 Free PMC article.

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