Garber A - Search Results

1

Prenatal diagnosis and dysmorphic findings in mosaic trisomy 16.

Garber A, Carlson D, Schreck R, Fischel-Ghodsian N, Hsu WT, Oeztas S, Pepkowitz S, Graham JM Jr. Garber A, et al. Prenat Diagn. 1994 Apr;14(4):257-66. doi: 10.1002/pd.1970140405. Prenat Diagn. 1994. PMID: 8066035

2

Fetal akinesia/hypokinesia sequence: prenatal diagnosis and intra-familial variability.

Bacino CA, Platt LD, Garber A, Carlson D, Pepkowitz S, Lachman RS, Sharony R, Rimoin DL, Graham JM Jr. Bacino CA, et al. Among authors: garber a. Prenat Diagn. 1993 Nov;13(11):1011-9. doi: 10.1002/pd.1970131102. Prenat Diagn. 1993. PMID: 8140062

3

Preaxial ray reduction defects as part of valproic acid embryofetopathy.

Sharony R, Garber A, Viskochil D, Schreck R, Platt LD, Ward R, Buehler BA, Graham JM Jr. Sharony R, et al. Among authors: garber a. Prenat Diagn. 1993 Oct;13(10):909-18. doi: 10.1002/pd.1970131005. Prenat Diagn. 1993. PMID: 8309898

4

Mosaic trisomy 16 ascertained through amniocentesis: evaluation of 11 new cases.

Hsu WT, Shchepin DA, Mao R, Berry-Kravis E, Garber AP, Fischel-Ghodsian N, Falk RE, Carlson DE, Roeder ER, Leeth EA, Hajianpour MJ, Wang JC, Rosenblum-Vos LS, Bhatt SD, Karson EM, Hux CH, Trunca C, Bialer MG, Linn SK, Schreck RR. Hsu WT, et al. Among authors: garber ap. Am J Med Genet. 1998 Dec 28;80(5):473-80. doi: 10.1002/(sici)1096-8628(19981228)80:5<473::aid-ajmg7>3.0.co;2-a. Am J Med Genet. 1998. PMID: 9880211

5

Determinants of utilization of Tay-Sachs screening.

Garber AP, Platt LD, Wang SJ, Jam K, Carlson DE, Rotter JI. Garber AP, et al. Obstet Gynecol. 1993 Sep;82(3):460-3. Obstet Gynecol. 1993. PMID: 8355954

6

Megacystis-microcolon-intestinal hypoperistalsis syndrome in two male siblings.

Garber A, Shohat M, Sarti D. Garber A, et al. Prenat Diagn. 1990 Jun;10(6):377-87. doi: 10.1002/pd.1970100605. Prenat Diagn. 1990. PMID: 2217079 Review.

7

Prenatal genetic counseling.

Garber AP, Hixon HE. Garber AP, et al. Clin Perinatol. 1990 Dec;17(4):749-59. Clin Perinatol. 1990. PMID: 2286025 Review.

8

Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19.

Briggs MD, Rasmussen IM, Weber JL, Yuen J, Reinker K, Garber AP, Rimoin DL, Cohn DH. Briggs MD, et al. Among authors: garber ap. Genomics. 1993 Dec;18(3):656-60. doi: 10.1016/s0888-7543(05)80369-6. Genomics. 1993. PMID: 8307576

9

Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22.

Krakow D, Reinker K, Powell B, Cantor R, Priore MA, Garber A, Lachman RS, Rimoin DL, Cohn DH. Krakow D, et al. Among authors: garber a. Am J Hum Genet. 1998 Jul;63(1):120-4. doi: 10.1086/301921. Am J Hum Genet. 1998. PMID: 9634519 Free PMC article.

10

Osteogenesis imperfecta type II delineation of the phenotype with reference to genetic heterogeneity.

Sillence DO, Barlow KK, Garber AP, Hall JG, Rimoin DL. Sillence DO, et al. Among authors: garber ap. Am J Med Genet. 1984 Feb;17(2):407-23. doi: 10.1002/ajmg.1320170204. Am J Med Genet. 1984. PMID: 6702894

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