Bull MJ - Search Results

1

Macrocephaly-cutis marmorata telangiectatica congenita: a distinct disorder with developmental delay and connective tissue abnormalities.

Moore CA, Toriello HV, Abuelo DN, Bull MJ, Curry CJ, Hall BD, Higgins JV, Stevens CA, Twersky S, Weksberg R, Dobyns WB. Moore CA, et al. Among authors: bull mj. Am J Med Genet. 1997 May 2;70(1):67-73. Am J Med Genet. 1997. PMID: 9129744

2

Familial occurrence of renal and Müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay.

Davee MA, Moore CA, Bull MJ, Hodes ME. Davee MA, et al. Among authors: bull mj. Am J Med Genet. 1992 Oct 1;44(3):293-6. doi: 10.1002/ajmg.1320440306. Am J Med Genet. 1992. PMID: 1283287

3

Fetal brain disruption sequence.

Moore CA, Weaver DD, Bull MJ. Moore CA, et al. Among authors: bull mj. J Pediatr. 1990 Mar;116(3):383-6. doi: 10.1016/s0022-3476(05)82825-2. J Pediatr. 1990. PMID: 2308027

4

Marshall-Smith syndrome: natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities.

Adam MP, Hennekam RC, Keppen LD, Bull MJ, Clericuzio CL, Burke LW, Ormond KE, Hoyme EH. Adam MP, et al. Among authors: bull mj. Am J Med Genet A. 2005 Aug 30;137(2):117-24. doi: 10.1002/ajmg.a.30580. Am J Med Genet A. 2005. PMID: 16086394 Review.

5

Lethal syndrome of skeletal dysplasia and progressive central nervous system degeneration.

Khosravi M, Weaver DD, Bull MJ, Lachman R, Rimoin DL. Khosravi M, et al. Among authors: bull mj. Am J Med Genet. 1998 Apr 28;77(1):63-71. Am J Med Genet. 1998. PMID: 9557897

6

Treatment of Smith-Lemli-Opitz syndrome: results of a multicenter trial.

Irons M, Elias ER, Abuelo D, Bull MJ, Greene CL, Johnson VP, Keppen L, Schanen C, Tint GS, Salen G. Irons M, et al. Among authors: bull mj. Am J Med Genet. 1997 Jan 31;68(3):311-4. Am J Med Genet. 1997. PMID: 9024565 Clinical Trial.

7

Urorectal septum malformation sequence: report of thirteen additional cases and review of the literature.

Wheeler PG, Weaver DD, Obeime MO, Vance GH, Bull MJ, Escobar LF. Wheeler PG, et al. Among authors: bull mj. Am J Med Genet. 1997 Dec 31;73(4):456-62. Am J Med Genet. 1997. PMID: 9415474 Review.

8

Antley-Bixler syndrome from a prognostic perspective: report of a case and review of the literature.

Escobar LF, Bixler D, Sadove M, Bull MJ. Escobar LF, et al. Among authors: bull mj. Am J Med Genet. 1988 Apr;29(4):829-36. doi: 10.1002/ajmg.1320290412. Am J Med Genet. 1988. PMID: 3041834 Review.

9

Gastrointestinal abnormalities: a significant cause of feeding difficulties and failure to thrive in Brachmann-de Lange syndrome.

Bull MJ, Fitzgerald JF, Heifetz SA, Brei TJ. Bull MJ, et al. Am J Med Genet. 1993 Nov 15;47(7):1029-34. doi: 10.1002/ajmg.1320470720. Am J Med Genet. 1993. PMID: 8291519

10

Clinical identification of feeding and swallowing disorders in 0-6 month old infants with Down syndrome.

Stanley MA, Shepherd N, Duvall N, Jenkinson SB, Jalou HE, Givan DC, Steele GH, Davis C, Bull MJ, Watkins DU, Roper RJ. Stanley MA, et al. Among authors: bull mj. Am J Med Genet A. 2019 Feb;179(2):177-182. doi: 10.1002/ajmg.a.11. Epub 2018 Dec 27. Am J Med Genet A. 2019. PMID: 30588741 Free PMC article.

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